A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv596288



Internal ID16383697
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:179870791..180070291hg38UCSC Ensembl
Innerchr4:180791944..180991444hg19UCSC Ensembl
Innerchr4:181028938..181228438hg18UCSC Ensembl
Cytoband4q34.3
Allele length
AssemblyAllele length
hg38199501
hg19199501
hg18199501
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1017053
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv596288
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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