A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1029680



Internal ID18772211
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:29865090..29909182hg38UCSC Ensembl
Innerchr6:29832867..29876959hg19UCSC Ensembl
Innerchr6:29940846..29984938hg18UCSC Ensembl
Cytoband6p21.33
Allele length
AssemblyAllele length
hg3844093
hg1944093
hg1844093
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5938n100
Supporting Variantsnssv3655767
Samples
Known GenesHLA-H
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1029680
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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