A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv697751



Internal ID15434403
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:114311045..114311308hg38UCSC Ensembl
Innerchr9:117073325..117073588hg19UCSC Ensembl
Innerchr9:116113146..116113409hg18UCSC Ensembl
Innerchr9:114152879..114153142hg17UCSC Ensembl
Cytoband9q32
Allele length
AssemblyAllele length
hg38264
hg19264
hg18264
hg17264
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv521043
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv697751
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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