A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv593905



Internal ID16381314
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:33316460..33370299hg38UCSC Ensembl
Innerchr4:33318082..33371921hg19UCSC Ensembl
Innerchr4:32994477..33048316hg18UCSC Ensembl
Cytoband4p15.1
Allele length
AssemblyAllele length
hg3853840
hg1953840
hg1853840
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv995201
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv593905
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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