A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1019395



Internal ID19108613
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:32486734..32657306hg38UCSC Ensembl
Innerchr6:32454511..32625083hg19UCSC Ensembl
Innerchr6:32562489..32733061hg18UCSC Ensembl
Cytoband6p21.32
Allele length
AssemblyAllele length
hg38170573
hg19170573
hg18170573
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3745469
Samples
Known GenesHLA-DQA1, HLA-DRB1, HLA-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)nsv1019395
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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