A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv520313



Internal ID15447606
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:98568774..98575382hg38UCSC Ensembl
Innerchr15:99112003..99118611hg19UCSC Ensembl
Innerchr15:96929526..96936134hg18UCSC Ensembl
Innerchr15:96929526..96936134hg17UCSC Ensembl
Cytoband15q26.3
Allele length
AssemblyAllele length
hg386609
hg196609
hg186609
hg176609
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv697342
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv520313
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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