A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv835291



Internal ID16129247
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:105738963..105739931hg38UCSC Ensembl
Innerchr14:106205300..106206268hg19UCSC Ensembl
Innerchr14:105276345..105277313hg18UCSC Ensembl
Cytoband14q32.33
Allele length
AssemblyAllele length
hg38969
hg19969
hg18969
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv566453
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)nssv835291
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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