A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv523314



Internal ID15450607
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:117003095..117046440hg38UCSC Ensembl
Innerchr3:116721942..116765287hg19UCSC Ensembl
Innerchr3:118204632..118247977hg18UCSC Ensembl
Innerchr3:118204632..118247977hg17UCSC Ensembl
Cytoband3q13.31
Allele length
AssemblyAllele length
hg3843346
hg1943346
hg1843346
hg1743346
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv699056
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv523314
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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