A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv593199



Internal ID16380608
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:337951..480163hg38UCSC Ensembl
Innerchr4:331740..473952hg19UCSC Ensembl
Innerchr4:321740..463952hg18UCSC Ensembl
Cytoband4p16.3
Allele length
AssemblyAllele length
hg38142213
hg19142213
hg18142213
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1153425
SamplesHGDP01369
Known GenesABCA11P, ZNF141, ZNF721
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv593199
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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