A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3595892



Internal ID6636166
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:37411389..37414092hg38UCSC Ensembl
Innerchr3:37411396..37414085hg38UCSC Ensembl
Outerchr3:37411382..37414099hg38UCSC Ensembl
chr3:37452880..37455583hg19UCSC Ensembl
Innerchr3:37452887..37455576hg19UCSC Ensembl
Outerchr3:37452873..37455590hg19UCSC Ensembl
Cytoband3p22.2
Allele length
AssemblyAllele length
hg382704
hg192704
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv10982681, essv10982711, essv10982670, essv10982697, essv10982723, essv10982724, essv10982717, essv10982745, essv10982716, essv10982673, essv10982721, essv10982746, essv10982715, essv10982685, essv10982698, essv10982735, essv10982728, essv10982664, essv10982668, essv10982703, essv10982742, essv10982683, essv10982706, essv10982743, essv10982686, essv10982725, essv10982694, essv10982701, essv10982713, essv10982692, essv10982702, essv10982719, essv10982708, essv10982704, essv10982734, essv10982714, essv10982727, essv10982659, essv10982712, essv10982672, essv10982662, essv10982657, essv10982678, essv10982661, essv10982675, essv10982679, essv10982744, essv10982695, essv10982682, essv10982733, essv10982710, essv10982700, essv10982737, essv10982720, essv10982726, essv10982732, essv10982738, essv10982666, essv10982677, essv10982699, essv10982740, essv10982674, essv10982696, essv10982729, essv10982707, essv10982658, essv10982687, essv10982705, essv10982739, essv10982669, essv10982688, essv10982690, essv10982741, essv10982691, essv10982663, essv10982736, essv10982665, essv10982684, essv10982718, essv10982676, essv10982731, essv10982689, essv10982722, essv10982730, essv10982709, essv10982680, essv10982693, essv10982667, essv10982671, essv10982660
SamplesHG02107, NA19625, NA18861, HG03567, HG02675, HG02970, HG03351, HG03521, NA19114, NA18874, HG03478, HG02983, NA19401, NA19149, NA20346, NA20299, NA19319, NA19334, HG03419, HG03212, HG03571, NA19449, NA18865, HG03048, NA18507, HG02760, NA19108, HG03485, NA19355, HG03378, NA19147, HG03049, HG03376, HG02895, NA19117, HG03461, HG03451, NA20356, NA19197, HG02568, NA19397, NA18876, NA19908, HG01396, HG03520, HG02851, HG03100, NA19835, HG01986, HG02756, HG02757, NA19247, HG03126, NA19153, NA19129, HG02449, HG02537, NA19372, HG03397, HG02562, HG03547, HG02623, HG03514, HG03096, HG02511, HG02771, HG03069, HG03428, HG02852, HG03157, NA19707, NA19159, HG03291, HG01894, NA19711, NA19141, HG02624, HG03224, NA19201, NA20274, NA19099, HG02465, NA19327, HG01886, HG02679, HG01892, NA19185, HG02820, NA19121, HG03082
Known GenesC3orf35
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3595892
Frequency
Sample Size2504
Observed Gain0
Observed Loss90
Observed Complex0
Frequencyn/a


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