A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv596332



Internal ID16383741
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:182958881..183011532hg38UCSC Ensembl
Innerchr4:183880034..183932685hg19UCSC Ensembl
Innerchr4:184117028..184169679hg18UCSC Ensembl
Cytoband4q35.1
Allele length
AssemblyAllele length
hg3852652
hg1952652
hg1852652
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1153518
Samples1780854537_A
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv596332
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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