A curated catalogue of human genomic structural variation

Variant Details

Variant: esv3623128

Internal ID6663296
Location Information
TypeCoordinatesAssemblyOther Links
chr10:46224802..46263254hg38UCSC Ensembl
chr10:47596038..47634490hg19UCSC Ensembl
Allele length
AssemblyAllele length
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13785609, essv13785597, essv13785584, essv13785641, essv13785615, essv13785639, essv13785638, essv13785607, essv13785642, essv13785585, essv13785600, essv13785630, essv13785617, essv13785621, essv13785644, essv13785596, essv13785619, essv13785637, essv13785624, essv13785601, essv13785612, essv13785590, essv13785635, essv13785643, essv13785623, essv13785610, essv13785636, essv13785594, essv13785633, essv13785640, essv13785593, essv13785614, essv13785620, essv13785592, essv13785613, essv13785629, essv13785618, essv13785634, essv13785583, essv13785628, essv13785595, essv13785632, essv13785616, essv13785631, essv13785608, essv13785611, essv13785589, essv13785591, essv13785599, essv13785604, essv13785625, essv13785626, essv13785606, essv13785602, essv13785598, essv13785587, essv13785627, essv13785605, essv13785588, essv13785586, essv13785603, essv13785622
SamplesHG02724, HG01776, NA19248, HG01515, NA18861, HG03521, NA20506, HG00551, HG02816, HG01882, HG03563, HG03410, HG02896, HG03196, NA20802, HG01051, NA19334, HG03709, NA19701, NA19474, HG03378, NA20755, NA19147, HG02973, NA20340, NA19043, HG02895, HG03558, HG04238, NA19984, NA11840, HG03052, HG00237, HG01986, HG03757, NA20587, NA19372, NA19384, NA18486, HG04080, HG02938, HG03740, NA18504, NA20818, HG02484, HG02301, NA19138, HG03499, NA19394, HG02688, HG01412, NA19452, HG01945, HG02678, HG02271, HG02721, NA19204, HG00671, NA18881, NA18519, NA20339, HG03095
Known GenesANTXRLP1
PlatformMultiple platforms
Pubmed ID21293372
Accession Number(s)esv3623128
Sample Size2504
Observed Gain0
Observed Loss62
Observed Complex0

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