A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv995919



Internal ID16289875
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:38663996..38664990hg38UCSC Ensembl
Innerchr4:38665617..38666611hg19UCSC Ensembl
Innerchr4:38342012..38343006hg18UCSC Ensembl
Cytoband4p14
Allele length
AssemblyAllele length
hg38995
hg19995
hg18995
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv594002
Supporting Variants
Samples
Known GenesFLJ13197, KLF3
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv995919
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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