A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv595926



Internal ID16383335
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:161024150..161108645hg38UCSC Ensembl
Innerchr4:161945302..162029797hg19UCSC Ensembl
Innerchr4:162164752..162249247hg18UCSC Ensembl
Cytoband4q32.2
Allele length
AssemblyAllele length
hg3884496
hg1984496
hg1884496
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1010251
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv595926
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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