A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1149510



Internal ID15881293
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:85983020..86020992hg38UCSC Ensembl
Innerchr14:86449364..86487336hg19UCSC Ensembl
Innerchr14:85519117..85557089hg18UCSC Ensembl
Cytoband14q31.3
Allele length
AssemblyAllele length
hg3837973
hg1937973
hg1837973
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv565455
Supporting Variants
SamplesNINDS_96
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1149510
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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