A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv697128



Internal ID15433780
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:7203306..7212446hg38UCSC Ensembl
Innerchr9:7203306..7212446hg19UCSC Ensembl
Innerchr9:7193306..7202446hg18UCSC Ensembl
Innerchr9:7193306..7202446hg17UCSC Ensembl
Cytoband9p24.1
Allele length
AssemblyAllele length
hg389141
hg199141
hg189141
hg179141
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv519922
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv697128
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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