A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv834408



Internal ID16128364
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:103847089..103848623hg38UCSC Ensembl
Innerchr14:104313426..104314960hg19UCSC Ensembl
Innerchr14:103383179..103384713hg18UCSC Ensembl
Cytoband14q32.33
Allele length
AssemblyAllele length
hg381535
hg191535
hg181535
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv566025
Supporting Variants
Samples
Known GenesLINC00637, PPP1R13B
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv834408
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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