A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv516436



Internal ID15443729
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:98710831..98727250hg38UCSC Ensembl
Innerchr14:99177168..99193587hg19UCSC Ensembl
Innerchr14:98246921..98263340hg18UCSC Ensembl
Innerchr14:98246921..98263340hg17UCSC Ensembl
Cytoband14q32.2
Allele length
AssemblyAllele length
hg3816420
hg1916420
hg1816420
hg1716420
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv658574, nssv675929, nssv657713, nssv668348, nssv659894, nssv690756, nssv673823, nssv692256, nssv663540, nssv690936
Samples
Known GenesC14orf177
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv516436
Frequency
Sample Size2026
Observed Gain0
Observed Loss10
Observed Complex0
Frequencyn/a


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