A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv521195



Internal ID15448488
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+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv705327, nssv684328, nssv692503, nssv700519, nssv691411, nssv693990
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv521195
Frequency
Sample Size2026
Observed Gain3
Observed Loss3
Observed Complex0
Frequencyn/a


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