A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv689848



Internal ID15426500
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:114562728..114576961hg38UCSC Ensembl
Innerchr9:117325008..117339241hg19UCSC Ensembl
Innerchr9:116364829..116379062hg18UCSC Ensembl
Innerchr9:114404562..114418795hg17UCSC Ensembl
Cytoband9q32
Allele length
AssemblyAllele length
hg3814234
hg1914234
hg1814234
hg1714234
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv516723
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv689848
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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