A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv656684



Internal ID15393336
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:11967114..12013711hg38UCSC Ensembl
Innerchr9:11967114..12013711hg19UCSC Ensembl
Innerchr9:11957114..12003711hg18UCSC Ensembl
Innerchr9:11957114..12003711hg17UCSC Ensembl
Cytoband9p23
Allele length
AssemblyAllele length
hg3846598
hg1946598
hg1846598
hg1746598
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv517379
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv656684
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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