A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv688980



Internal ID15425632
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:8009428..8021219hg38UCSC Ensembl
Innerchr9:8009428..8021219hg19UCSC Ensembl
Innerchr9:7999428..8011219hg18UCSC Ensembl
Innerchr9:7999428..8011219hg17UCSC Ensembl
Cytoband9p24.1
Allele length
AssemblyAllele length
hg3811792
hg1911792
hg1811792
hg1711792
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv519428
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv688980
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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