A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2666334



Internal ID9932439
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:10657383..10659789hg38UCSC Ensembl
Outerchr6:10657012..10660159hg38UCSC Ensembl
Innerchr6:10657616..10660022hg19UCSC Ensembl
Outerchr6:10657245..10660392hg19UCSC Ensembl
Cytoband6p24.2
Allele length
AssemblyAllele length
hg383148
hg193148
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1075e199
Supporting Variantsessv5802329, essv5750792, essv6231330, essv5812115, essv6443493, essv5708204, essv5525364, essv6016519, essv5887099, essv6106325, essv5430686, essv5601591, essv5527871, essv5411625, essv6490286, essv6464957, essv5875525, essv6130854, essv6517716, essv5462035, essv6224009, essv6259750, essv5466289, essv5527878, essv5818459
SamplesHG00626, HG00542, HG00442, HG00671, HG00566, HG00654, HG00693, HG00501, HG00512, HG00683, HG00629, HG00596, HG00428, HG00653, HG00657, HG00708, HG00525, HG00704, HG00625, HG00607, HG00662, HG00656, HG00628, HG00437, HG00581
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2666334
Frequency
Sample Size1151
Observed Gain0
Observed Loss25
Observed Complex0
Frequencyn/a


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