A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv524615



Internal ID15451908
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:26804683..26856331hg38UCSC Ensembl
Innerchr3:26846174..26897822hg19UCSC Ensembl
Innerchr3:26821178..26872826hg18UCSC Ensembl
Innerchr3:26821178..26872826hg17UCSC Ensembl
Cytoband3p24.1
Allele length
AssemblyAllele length
hg3851649
hg1951649
hg1851649
hg1751649
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv700576
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv524615
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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