A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv525435



Internal ID15452728
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:34656805..34677308hg38UCSC Ensembl
Innerchr3:34698297..34718800hg19UCSC Ensembl
Innerchr3:34673301..34693804hg18UCSC Ensembl
Innerchr3:34673301..34693804hg17UCSC Ensembl
Cytoband3p22.3
Allele length
AssemblyAllele length
hg3820504
hg1920504
hg1820504
hg1720504
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv701563
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv525435
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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