A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv596524



Internal ID16037247
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:189113137..189856905hg38UCSC Ensembl
Innerchr4:190034291..190778060hg19UCSC Ensembl
Innerchr4:190271285..191015054hg18UCSC Ensembl
Cytoband4q35.2
Allele length
AssemblyAllele length
hg38743769
hg19743770
hg18743770
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv9457n54
Supporting Variantsnssv1020617
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv596524
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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