A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1019411



Internal ID19108629
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:32480822..32559495hg38UCSC Ensembl
Innerchr6:32448599..32527272hg19UCSC Ensembl
Innerchr6:32556577..32635250hg18UCSC Ensembl
Cytoband6p21.32
Allele length
AssemblyAllele length
hg3878674
hg1978674
hg1878674
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5948n100
Supporting Variantsnssv3655958, nssv3655956, nssv3655957, nssv3745378
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)nsv1019411
Frequency
Sample Size11257
Observed Gain4
Observed Loss0
Observed Complex0
Frequencyn/a


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