A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv518101



Internal ID15445394
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:161384309..161385073hg38UCSC Ensembl
Innerchr3:161102097..161102861hg19UCSC Ensembl
Innerchr3:162584791..162585555hg18UCSC Ensembl
Innerchr3:162584799..162585563hg17UCSC Ensembl
Cytoband3q26.1
Allele length
AssemblyAllele length
hg38765
hg19765
hg18765
hg17765
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv695514
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv518101
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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