A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1148709



Internal ID15854736
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:104276611..104335962hg38UCSC Ensembl
Innerchr14:104742948..104802299hg19UCSC Ensembl
Innerchr14:103813993..103873344hg18UCSC Ensembl
Cytoband14q32.33
Allele length
AssemblyAllele length
hg3859352
hg1959352
hg1859352
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv566040
Supporting Variants
Samples1780862306_A
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1148709
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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