A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv993067



Internal ID16287023
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:12124189..12199378hg38UCSC Ensembl
Innerchr4:12125813..12201002hg19UCSC Ensembl
Innerchr4:11734911..11810100hg18UCSC Ensembl
Cytoband4p15.33
Allele length
AssemblyAllele length
hg3875190
hg1975190
hg1875190
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv593742
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)nssv993067
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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