A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv833737



Internal ID16127693
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:101702580..101720203hg38UCSC Ensembl
Innerchr14:102168917..102186540hg19UCSC Ensembl
Innerchr14:101238670..101256293hg18UCSC Ensembl
Cytoband14q32.31
Allele length
AssemblyAllele length
hg3817624
hg1917624
hg1817624
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv565887
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)nssv833737
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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