A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv594818



Internal ID16382227
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:89651171..89703702hg38UCSC Ensembl
Innerchr4:90572322..90624853hg19UCSC Ensembl
Innerchr4:90791345..90843876hg18UCSC Ensembl
Cytoband4q22.1
Allele length
AssemblyAllele length
hg3852532
hg1952532
hg1852532
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv9158n54
Supporting Variantsnssv1153473, nssv1153474
SamplesHGDP00392, HGDP00359
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv594818
Frequency
Sample Size17421
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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