A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv527368



Internal ID15454661
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:29742063..29744927hg38UCSC Ensembl
Innerchr6:29709840..29712704hg19UCSC Ensembl
Innerchr6:29817819..29820683hg18UCSC Ensembl
Innerchr6:29817819..29820683hg17UCSC Ensembl
Cytoband6p22.1
Allele length
AssemblyAllele length
hg382865
hg192865
hg182865
hg172865
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv703799
Samples
Known GenesHLA-F-AS1
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv527368
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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