A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv528597



Internal ID15455890
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:59975788..59977405hg38UCSC Ensembl
Innerchr3:59961514..59963131hg19UCSC Ensembl
Innerchr3:59936554..59938171hg18UCSC Ensembl
Innerchr3:59936554..59938171hg17UCSC Ensembl
Cytoband3p14.2
Allele length
AssemblyAllele length
hg381618
hg191618
hg181618
hg171618
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv705223
Samples
Known GenesFHIT
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv528597
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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