A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv520641



Internal ID15447934
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:21163169..21164272hg38UCSC Ensembl
Innerchr14:21631328..21632431hg19UCSC Ensembl
Innerchr14:20701168..20702271hg18UCSC Ensembl
Innerchr14:20701168..20702271hg17UCSC Ensembl
Cytoband14q11.2
Allele length
AssemblyAllele length
hg381104
hg191104
hg181104
hg171104
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv697533
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv520641
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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