A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv657928



Internal ID15394580
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:113641805..113644764hg38UCSC Ensembl
Innerchr9:116404085..116407044hg19UCSC Ensembl
Innerchr9:115443906..115446865hg18UCSC Ensembl
Innerchr9:113483639..113486598hg17UCSC Ensembl
Cytoband9q32
Allele length
AssemblyAllele length
hg382960
hg192960
hg182960
hg172960
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv516235
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv657928
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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