A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv593492



Internal ID16380901
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:5783715..5814202hg38UCSC Ensembl
Innerchr4:5785442..5815929hg19UCSC Ensembl
Innerchr4:5836343..5866830hg18UCSC Ensembl
Cytoband4p16.1
Allele length
AssemblyAllele length
hg3830488
hg1930488
hg1830488
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv989316
Samples
Known GenesEVC
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv593492
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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