A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv593351



Internal ID16034074
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:1870705..1872093hg38UCSC Ensembl
Innerchr4:1872432..1873820hg19UCSC Ensembl
Innerchr4:1842230..1843618hg18UCSC Ensembl
Cytoband4p16.3
Allele length
AssemblyAllele length
hg381389
hg191389
hg181389
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv8903n54
Supporting Variantsnssv988475, nssv988474, nssv988471, nssv988477, nssv988473, nssv988476, nssv988472
Samples
Known GenesWHSC1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv593351
Frequency
Sample Size17421
Observed Gain7
Observed Loss0
Observed Complex0
Frequencyn/a


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