A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2674901



Internal ID9594320
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:32554086..32580931hg38UCSC Ensembl
Outerchr6:32554039..32581012hg38UCSC Ensembl
Innerchr6:32521863..32548708hg19UCSC Ensembl
Outerchr6:32521816..32548789hg19UCSC Ensembl
Cytoband6p21.32
Allele length
AssemblyAllele length
hg3826974
hg1926974
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1108e199
Supporting Variantsessv5467242, essv6218409, essv6530091, essv6589627, essv5865362, essv5456656, essv6236886, essv5751627, essv5844475, essv5410840, essv6043519, essv6158982, essv6385820, essv5804590, essv6212194, essv5941282, essv6126927, essv6035381, essv5907677, essv5524771, essv6081637, essv5696998, essv5945734, essv6136150, essv5649272, essv5516208, essv6089285, essv5531839, essv6291118, essv6122203, essv6117726, essv6423323, essv6584066, essv6528386, essv5581530, essv5939591, essv6551669, essv5656457, essv5604243
SamplesNA19066, HG00524, NA20802, NA19068, HG01366, NA18597, NA18567, NA11918, NA12283, NA20513, NA18964, HG01134, HG00277, HG00335, NA20340, HG00160, NA18557, HG00326, NA19789, HG00264, NA20535, NA19670, NA12342, NA18516, NA18534, NA19774, NA19000, NA18858, NA19675, HG01075, NA18909, NA18517, NA20504, HG00131, NA19661, NA11892, HG01082, HG00437, NA20772
Known GenesHLA-DRB1, HLA-DRB6
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2674901
Frequency
Sample Size1151
Observed Gain0
Observed Loss39
Observed Complex0
Frequencyn/a


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