A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv593793



Internal ID16381202
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:20280711..20332099hg38UCSC Ensembl
Innerchr4:20282334..20333722hg19UCSC Ensembl
Innerchr4:19891432..19942820hg18UCSC Ensembl
Cytoband4p15.31
Allele length
AssemblyAllele length
hg3851389
hg1951389
hg1851389
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv994227
Samples
Known GenesSLIT2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv593793
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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