A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv826031



Internal ID16119987
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:38489763..38605974hg38UCSC Ensembl
Innerchr14:38958967..39075178hg19UCSC Ensembl
Innerchr14:38028718..38144929hg18UCSC Ensembl
Cytoband14q21.1
Allele length
AssemblyAllele length
hg38116212
hg19116212
hg18116212
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv564415
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)nssv826031
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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