A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv594332



Internal ID16035055
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:62111038..62168356hg38UCSC Ensembl
Innerchr4:62976756..63034074hg19UCSC Ensembl
Innerchr4:62659351..62716669hg18UCSC Ensembl
Cytoband4q13.1
Allele length
AssemblyAllele length
hg3857319
hg1957319
hg1857319
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1000257
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv594332
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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