A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv593792



Internal ID16034515
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:20273854..20361093hg38UCSC Ensembl
Innerchr4:20275477..20362716hg19UCSC Ensembl
Innerchr4:19884575..19971814hg18UCSC Ensembl
Cytoband4p15.31
Allele length
AssemblyAllele length
hg3887240
hg1987240
hg1887240
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv994226
Samples
Known GenesSLIT2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv593792
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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