A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv828828



Internal ID16122784
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:70220199..70222555hg38UCSC Ensembl
Innerchr14:70686916..70689272hg19UCSC Ensembl
Innerchr14:69756669..69759025hg18UCSC Ensembl
Cytoband14q24.2
Allele length
AssemblyAllele length
hg382357
hg192357
hg182357
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv565011
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)nssv828828
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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