A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv596093



Internal ID16383502
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:167475570..167705288hg38UCSC Ensembl
Innerchr4:168396721..168626439hg19UCSC Ensembl
Innerchr4:168633296..168863014hg18UCSC Ensembl
Cytoband4q32.3
Allele length
AssemblyAllele length
hg38229719
hg19229719
hg18229719
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1152843
SamplesNINDS_160
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv596093
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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