A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv523715



Internal ID15451008
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:48451683..48499004hg38UCSC Ensembl
Innerchr14:48920886..48968207hg19UCSC Ensembl
Innerchr14:47990636..48037957hg18UCSC Ensembl
Innerchr14:47990636..48037957hg17UCSC Ensembl
Cytoband14q21.3
Allele length
AssemblyAllele length
hg3847322
hg1947322
hg1847322
hg1747322
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv699528
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv523715
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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