A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv519548



Internal ID15446841
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:34642506..34677308hg38UCSC Ensembl
Innerchr3:34683998..34718800hg19UCSC Ensembl
Innerchr3:34659002..34693804hg18UCSC Ensembl
Innerchr3:34659002..34693804hg17UCSC Ensembl
Cytoband3p22.3
Allele length
AssemblyAllele length
hg3834803
hg1934803
hg1834803
hg1734803
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv696914
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv519548
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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