A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv828830



Internal ID16122786
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:70220199..70222673hg38UCSC Ensembl
Innerchr14:70686916..70689390hg19UCSC Ensembl
Innerchr14:69756669..69759143hg18UCSC Ensembl
Cytoband14q24.2
Allele length
AssemblyAllele length
hg382475
hg192475
hg182475
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv565013
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)nssv828830
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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