A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv523740



Internal ID15451033
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:5053851..5110652hg38UCSC Ensembl
Innerchr1:5113911..5170712hg19UCSC Ensembl
Innerchr1:5013771..5070572hg18UCSC Ensembl
Innerchr1:5024284..5081085hg17UCSC Ensembl
Cytoband1p36.32
Allele length
AssemblyAllele length
hg3856802
hg1956802
hg1856802
hg1756802
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv699556
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv523740
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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