A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv695734



Internal ID15432386
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:170254992..170257897hg38UCSC Ensembl
Innerchr6:170564080..170566985hg19UCSC Ensembl
Innerchr6:170406005..170408910hg18UCSC Ensembl
Innerchr6:170481712..170484617hg17UCSC Ensembl
Cytoband6q27
Allele length
AssemblyAllele length
hg382906
hg192906
hg182906
hg172906
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv518303
Supporting Variants
Samples
Known GenesLOC154449
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv695734
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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