A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1024429



Internal ID18766961
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:32997190..33154554hg38UCSC Ensembl
Innerchr6:32964967..33122331hg19UCSC Ensembl
Innerchr6:33072945..33230309hg18UCSC Ensembl
Cytoband6p21.32
Allele length
AssemblyAllele length
hg38157365
hg19157365
hg18157365
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3745472, nssv3657341
Samples
Known GenesHLA-DOA, HLA-DPA1, HLA-DPB1, HLA-DPB2
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1024429
Frequency
Sample Size29084
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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