A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv699042



Internal ID15435694
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:34640765..34664427hg38UCSC Ensembl
Innerchr17:32967784..32991446hg19UCSC Ensembl
Innerchr17:29991897..30015559hg18UCSC Ensembl
Innerchr17:29991897..30015559hg17UCSC Ensembl
Cytoband17q12
Allele length
AssemblyAllele length
hg3823663
hg1923663
hg1823663
hg1723663
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv523302
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv699042
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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