A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv702472



Internal ID15439124
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:113641805..113642423hg38UCSC Ensembl
Innerchr9:116404085..116404703hg19UCSC Ensembl
Innerchr9:115443906..115444524hg18UCSC Ensembl
Innerchr9:113483639..113484257hg17UCSC Ensembl
Cytoband9q32
Allele length
AssemblyAllele length
hg38619
hg19619
hg18619
hg17619
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)nssv702472
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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