A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv691411



Internal ID15428063
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:23073970..23117289hg38UCSC Ensembl
Innerchr9:23073969..23117288hg19UCSC Ensembl
Innerchr9:23063969..23107288hg18UCSC Ensembl
Innerchr9:23063969..23107288hg17UCSC Ensembl
Cytoband9p21.3
Allele length
AssemblyAllele length
hg3843320
hg1943320
hg1843320
hg1743320
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv521195
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv691411
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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