A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv698165



Internal ID15434817
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:7913952..7919153hg38UCSC Ensembl
Innerchr9:7913952..7919153hg19UCSC Ensembl
Innerchr9:7903952..7909153hg18UCSC Ensembl
Innerchr9:7903952..7909153hg17UCSC Ensembl
Cytoband9p24.1
Allele length
AssemblyAllele length
hg385202
hg195202
hg185202
hg175202
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv521550
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv698165
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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