A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv524379



Internal ID15451672
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:5658445..5900299hg38UCSC Ensembl
Innerchr3:5700132..5941986hg19UCSC Ensembl
Innerchr3:5675132..5916986hg18UCSC Ensembl
Innerchr3:5675132..5916986hg17UCSC Ensembl
Cytoband3p26.1
Allele length
AssemblyAllele length
hg38241855
hg19241855
hg18241855
hg17241855
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv700294
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv524379
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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