A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv688827



Internal ID15425479
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:11847376..11919732hg38UCSC Ensembl
Innerchr9:11847376..11919732hg19UCSC Ensembl
Innerchr9:11837376..11909732hg18UCSC Ensembl
Innerchr9:11837376..11909732hg17UCSC Ensembl
Cytoband9p23
Allele length
AssemblyAllele length
hg3872357
hg1972357
hg1872357
hg1772357
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv517379
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv688827
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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