A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv517473



Internal ID15444766
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:22990403..22990849hg38UCSC Ensembl
Innerchr3:23031894..23032340hg19UCSC Ensembl
Innerchr3:23006898..23007344hg18UCSC Ensembl
Innerchr3:23006898..23007344hg17UCSC Ensembl
Cytoband3p24.3
Allele length
AssemblyAllele length
hg38447
hg19447
hg18447
hg17447
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv672355, nssv656899, nssv678438, nssv670719, nssv682269, nssv655369, nssv652121, nssv678277, nssv666763, nssv664828, nssv700934, nssv687159, nssv682239, nssv655012, nssv652940, nssv653340
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv517473
Frequency
Sample Size2026
Observed Gain1
Observed Loss15
Observed Complex0
Frequencyn/a


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