A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv518995



Internal ID15446288
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:37911103..37919100hg38UCSC Ensembl
Innerchr3:37952594..37960591hg19UCSC Ensembl
Innerchr3:37927598..37935595hg18UCSC Ensembl
Innerchr3:37927598..37935595hg17UCSC Ensembl
Cytoband3p22.2
Allele length
AssemblyAllele length
hg387998
hg197998
hg187998
hg177998
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv696462
Samples
Known GenesCTDSPL
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv518995
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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