A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1017057



Internal ID16311013
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:180567916..180619604hg38UCSC Ensembl
Innerchr4:181489069..181540757hg19UCSC Ensembl
Innerchr4:181726063..181777751hg18UCSC Ensembl
Cytoband4q34.3
Allele length
AssemblyAllele length
hg3851689
hg1951689
hg1851689
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv596295
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)nssv1017057
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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