A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv832747



Internal ID16126703
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:98703993..98731630hg38UCSC Ensembl
Innerchr14:99170330..99197967hg19UCSC Ensembl
Innerchr14:98240083..98267720hg18UCSC Ensembl
Cytoband14q32.2
Allele length
AssemblyAllele length
hg3827638
hg1927638
hg1827638
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv565667
Supporting Variants
Samples
Known GenesC14orf177
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv832747
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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