A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv593198



Internal ID16033921
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:288710..425776hg38UCSC Ensembl
Innerchr4:282499..419565hg19UCSC Ensembl
Innerchr4:272499..409565hg18UCSC Ensembl
Cytoband4p16.3
Allele length
AssemblyAllele length
hg38137067
hg19137067
hg18137067
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv987405
Samples
Known GenesABCA11P, ZNF141, ZNF732
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv593198
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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