A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv518580



Internal ID15445873
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:184388705..184403023hg38UCSC Ensembl
Innerchr3:184106493..184120811hg19UCSC Ensembl
Innerchr3:185589187..185603505hg18UCSC Ensembl
Innerchr3:185589195..185603513hg17UCSC Ensembl
Cytoband3q27.1
Allele length
AssemblyAllele length
hg3814319
hg1914319
hg1814319
hg1714319
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv696024
Samples
Known GenesCHRD
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv518580
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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