A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3622418



Internal ID6662588
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:14199695..14200437hg38UCSC Ensembl
Innerchr10:14199695..14200437hg38UCSC Ensembl
Outerchr10:14199485..14200689hg38UCSC Ensembl
chr10:14241694..14242436hg19UCSC Ensembl
Innerchr10:14241694..14242436hg19UCSC Ensembl
Outerchr10:14241484..14242688hg19UCSC Ensembl
Cytoband10p13
Allele length
AssemblyAllele length
hg38743
hg19743
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13700573, essv13700632, essv13700601, essv13700607, essv13700590, essv13700683, essv13700660, essv13700662, essv13700557, essv13700682, essv13700686, essv13700628, essv13700602, essv13700561, essv13700685, essv13700637, essv13700653, essv13700609, essv13700594, essv13700571, essv13700620, essv13700672, essv13700581, essv13700553, essv13700576, essv13700641, essv13700633, essv13700554, essv13700555, essv13700687, essv13700592, essv13700689, essv13700589, essv13700558, essv13700583, essv13700578, essv13700629, essv13700586, essv13700678, essv13700618, essv13700563, essv13700570, essv13700595, essv13700623, essv13700677, essv13700691, essv13700587, essv13700579, essv13700608, essv13700612, essv13700681, essv13700622, essv13700666, essv13700619, essv13700621, essv13700658, essv13700663, essv13700668, essv13700636, essv13700638, essv13700610, essv13700684, essv13700616, essv13700580, essv13700606, essv13700675, essv13700690, essv13700674, essv13700566, essv13700582, essv13700646, essv13700656, essv13700588, essv13700639, essv13700659, essv13700654, essv13700598, essv13700624, essv13700614, essv13700676, essv13700625, essv13700560, essv13700626, essv13700640, essv13700599, essv13700569, essv13700577, essv13700651, essv13700597, essv13700635, essv13700630, essv13700615, essv13700634, essv13700565, essv13700643, essv13700559, essv13700671, essv13700649, essv13700650, essv13700642, essv13700596, essv13700631, essv13700605, essv13700645, essv13700679, essv13700669, essv13700613, essv13700568, essv13700562, essv13700591, essv13700688, essv13700652, essv13700670, essv13700680, essv13700647, essv13700665, essv13700567, essv13700648, essv13700604, essv13700572, essv13700664, essv13700564, essv13700661, essv13700667, essv13700584, essv13700556, essv13700611, essv13700600, essv13700593, essv13700627, essv13700673, essv13700617, essv13700655, essv13700603, essv13700575, essv13700644, essv13700574, essv13700585, essv13700657
SamplesHG00323, HG01864, HG00309, HG01515, HG03963, NA12718, HG00313, NA12249, HG01790, HG00304, HG01104, HG01603, NA19089, HG00234, HG04156, NA19081, HG00350, HG01089, HG03711, NA11920, HG00171, HG00112, HG01105, HG00384, NA10847, NA12340, HG01624, NA18948, HG00463, HG00189, NA20800, NA18953, HG03829, NA18947, NA19010, HG00375, NA20321, HG00106, HG02676, HG00334, NA07051, HG00280, HG00557, HG01608, NA12287, NA18943, NA18950, HG00188, HG00256, NA12414, HG00115, HG00154, HG01765, HG00339, HG00158, HG02390, NA19067, NA12763, NA20854, HG00371, HG01092, NA18992, HG00421, HG00240, NA20811, HG02121, HG01756, HG02658, HG03436, HG01124, HG00628, NA19066, HG00338, HG02220, NA12829, NA20520, NA11995, HG03917, NA19056, HG00357, NA18643, HG00133, HG00114, HG00436, HG02236, HG01810, NA18645, HG02541, NA06985, HG00185, NA20795, NA18968, NA18986, HG01486, NA19005, HG00273, NA19704, NA20814, HG00102, NA18564, NA18942, NA19001, HG00341, HG00105, NA19074, HG01512, HG00109, HG02219, NA18619, NA18582, NA20827, NA06984, NA19009, NA12156, HG02230, NA18971, HG00311, NA18602, NA20507, NA18548, NA19740, NA12399, HG00238, HG00656, HG01058, HG01119, NA19756, HG00288, HG03802, NA18574, NA21105, HG00183, NA19079, HG01479, HG00376, NA19087, NA19007, HG00107, HG01686
Known GenesFRMD4A
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3622418
Frequency
Sample Size2504
Observed Gain0
Observed Loss139
Observed Complex0
Frequencyn/a


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