A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1029001



Internal ID19118220
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:32480822..32562509hg38UCSC Ensembl
Innerchr6:32448599..32530286hg19UCSC Ensembl
Innerchr6:32556577..32638264hg18UCSC Ensembl
Cytoband6p21.32
Allele length
AssemblyAllele length
hg3881688
hg1981688
hg1881688
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5949n100
Supporting Variantsnssv3655960, nssv3655959
Samples
Known GenesHLA-DRB5, HLA-DRB6
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1029001
Frequency
Sample Size11257
Observed Gain1
Observed Loss1
Observed Complex0
Frequencyn/a


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