A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv834063



Internal ID16128019
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:101711842..101727209hg38UCSC Ensembl
Innerchr14:102178179..102193546hg19UCSC Ensembl
Innerchr14:101247932..101263299hg18UCSC Ensembl
Cytoband14q32.31
Allele length
AssemblyAllele length
hg3815368
hg1915368
hg1815368
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv565910
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)nssv834063
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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