A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv832162



Internal ID15779432
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:87497542..87928587hg38UCSC Ensembl
Innerchr14:87963886..88394931hg19UCSC Ensembl
Innerchr14:87033639..87464684hg18UCSC Ensembl
Cytoband14q31.3
Allele length
AssemblyAllele length
hg38431046
hg19431046
hg18431046
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv565504
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv832162
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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