A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3657338



Internal ID18955619
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:32640300..32711222hg38UCSC Ensembl
Innerchr6:32608077..32678999hg19UCSC Ensembl
Innerchr6:32716055..32786977hg18UCSC Ensembl
Cytoband6p21.32
Allele length
AssemblyAllele length
hg3870923
hg1970923
hg1870923
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1017819
Supporting Variants
Samples
Known GenesHLA-DQA1, HLA-DQB1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3657338
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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