A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv523719



Internal ID15451012
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:75359756..75364418hg38UCSC Ensembl
Innerchr14:75826459..75831121hg19UCSC Ensembl
Innerchr14:74896212..74900874hg18UCSC Ensembl
Innerchr14:74896212..74900874hg17UCSC Ensembl
Cytoband14q24.3
Allele length
AssemblyAllele length
hg384663
hg194663
hg184663
hg174663
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv699533
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv523719
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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