A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv521040



Internal ID15101647
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:147182..179398hg38UCSC Ensembl
Innerchr3:188865..221081hg19UCSC Ensembl
Innerchr3:163865..196081hg18UCSC Ensembl
Innerchr3:163865..196081hg17UCSC Ensembl
Cytoband3p26.3
Allele length
AssemblyAllele length
hg3832217
hg1932217
hg1832217
hg1732217
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv680470, nssv691425, nssv701024
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv521040
Frequency
Sample Size2026
Observed Gain1
Observed Loss2
Observed Complex0
Frequencyn/a


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