A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv666982



Internal ID15403634
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:113641805..113643288hg38UCSC Ensembl
Innerchr9:116404085..116405568hg19UCSC Ensembl
Innerchr9:115443906..115445389hg18UCSC Ensembl
Innerchr9:113483639..113485122hg17UCSC Ensembl
Cytoband9q32
Allele length
AssemblyAllele length
hg381484
hg191484
hg181484
hg171484
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)nssv666982
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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