A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2660354



Internal ID9579773
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:25902439..25902637hg38UCSC Ensembl
chr21:27274751..27274949hg19UCSC Ensembl
Cytoband21q21.3
Allele length
AssemblyAllele length
hg38199
hg19199
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv5706888, essv6136539, essv5771937, essv5802560, essv6473779, essv5994916, essv5743123, essv6570537, essv5887933, essv6032425, essv5480239, essv6365583, essv5921996, essv5717438, essv5913906, essv6007849, essv5715497, essv6164699, essv6445461, essv6289941, essv5622234, essv5953251, essv6360763, essv6353232, essv6498582, essv5776692, essv6055640, essv6439319, essv6040978, essv6328234, essv5798881, essv5982591, essv6182522, essv6563739, essv5952344, essv6069853, essv6591006, essv5710581, essv6035150, essv5513952, essv6293493, essv6481927, essv6352582, essv5475459, essv6051873, essv6168123, essv6557295, essv6550977, essv5649477, essv5623741, essv5619845, essv6284323, essv6035278, essv6021009, essv6028009, essv6563148, essv5801069, essv5716667, essv5650571, essv6433737, essv6054382, essv5653988, essv6508347, essv5594185, essv5597431, essv6148450, essv5934878, essv6425159, essv5825240, essv6192768, essv5404260
SamplesHG01441, HG00537, HG00536, HG00607, HG01440, NA18951, HG00418, HG00705, HG01083, NA18612, NA18526, NA18550, NA18545, NA18603, NA18948, HG00463, HG00614, NA18573, NA18542, NA18546, HG00701, HG00651, HG00557, HG00699, NA18557, NA18943, HG00353, NA18949, NA18632, HG00543, HG01107, HG01384, HG00421, NA18635, NA18536, NA18622, NA18563, HG00692, HG00689, NA18638, NA18956, NA18959, NA18609, NA18547, NA18637, NA18973, NA19663, NA19657, NA19731, NA18558, HG00672, HG01356, NA18613, HG00525, NA18562, NA18579, NA18597, HG00580, HG00608, HG00654, HG00530, HG00656, HG00422, HG00708, NA18611, HG00690, HG00684, HG00671, HG00702, NA18555, HG00531
Known GenesAPP
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2660354
Frequency
Sample Size1151
Observed Gain0
Observed Loss71
Observed Complex0
Frequencyn/a


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