A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv989093



Internal ID16283049
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:2535901..2537514hg38UCSC Ensembl
Innerchr4:2537628..2539241hg19UCSC Ensembl
Innerchr4:2507426..2509039hg18UCSC Ensembl
Cytoband4p16.3
Allele length
AssemblyAllele length
hg381614
hg191614
hg181614
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv593424
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv989093
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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