A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1020872



Internal ID16314828
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:189492254..189826984hg38UCSC Ensembl
Innerchr4:190413408..190748138hg19UCSC Ensembl
Innerchr4:190650402..190985132hg18UCSC Ensembl
Cytoband4q35.2
Allele length
AssemblyAllele length
hg38334731
hg19334731
hg18334731
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv596554
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)nssv1020872
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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