A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv596196



Internal ID16383605
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:171631808..171764944hg38UCSC Ensembl
Innerchr4:172552959..172686095hg19UCSC Ensembl
Innerchr4:172789534..172922670hg18UCSC Ensembl
Cytoband4q34.1
Allele length
AssemblyAllele length
hg38133137
hg19133137
hg18133137
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1014364
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv596196
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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