A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1022506



Internal ID19111724
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:32461942..32550980hg38UCSC Ensembl
Innerchr6:32429719..32518757hg19UCSC Ensembl
Innerchr6:32537697..32626735hg18UCSC Ensembl
Cytoband6p21.32
Allele length
AssemblyAllele length
hg3889039
hg1989039
hg1889039
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5946n100
Supporting Variantsnssv3655914, nssv3745374, nssv3655915, nssv3655913
Samples
Known GenesHLA-DRB5
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1022506
Frequency
Sample Size11257
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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