A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv596441



Internal ID16383850
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:186774410..186865162hg38UCSC Ensembl
Innerchr4:187695564..187786316hg19UCSC Ensembl
Innerchr4:187932558..188023310hg18UCSC Ensembl
Cytoband4q35.2
Allele length
AssemblyAllele length
hg3890753
hg1990753
hg1890753
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1020477
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv596441
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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