A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv517535



Internal ID15444828
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:191926682..191957971hg38UCSC Ensembl
Innerchr3:191644471..191675760hg19UCSC Ensembl
Innerchr3:193127165..193158454hg18UCSC Ensembl
Innerchr3:193127173..193158462hg17UCSC Ensembl
Cytoband3q28
Allele length
AssemblyAllele length
hg3831290
hg1931290
hg1831290
hg1731290
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv652939, nssv652290, nssv683897, nssv699797, nssv689542, nssv662771
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv517535
Frequency
Sample Size2026
Observed Gain0
Observed Loss6
Observed Complex0
Frequencyn/a


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