A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv832691



Internal ID16126647
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:93988523..93998001hg38UCSC Ensembl
Innerchr14:94454869..94464347hg19UCSC Ensembl
Innerchr14:93524622..93534100hg18UCSC Ensembl
Cytoband14q32.12
Allele length
AssemblyAllele length
hg389479
hg199479
hg189479
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv565617
Supporting Variants
Samples
Known GenesLINC00521
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv832691
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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