A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv593433



Internal ID16380842
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:2536427..2548745hg38UCSC Ensembl
Innerchr4:2538154..2550472hg19UCSC Ensembl
Innerchr4:2507952..2520270hg18UCSC Ensembl
Cytoband4p16.3
Allele length
AssemblyAllele length
hg3812319
hg1912319
hg1812319
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv8920n54
Supporting Variantsnssv989110
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv593433
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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