A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv526437



Internal ID15453730
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:72322374..72329582hg38UCSC Ensembl
Innerchr3:72371525..72378733hg19UCSC Ensembl
Innerchr3:72454215..72461423hg18UCSC Ensembl
Innerchr3:72454215..72461423hg17UCSC Ensembl
Cytoband3p13
Allele length
AssemblyAllele length
hg387209
hg197209
hg187209
hg177209
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv702740
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv526437
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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