A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv594819



Internal ID16382228
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:89651171..89709750hg38UCSC Ensembl
Innerchr4:90572322..90630901hg19UCSC Ensembl
Innerchr4:90791345..90849924hg18UCSC Ensembl
Cytoband4q22.1
Allele length
AssemblyAllele length
hg3858580
hg1958580
hg1858580
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv9158n54
Supporting Variantsnssv1153475
SamplesHGDP00351
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv594819
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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