A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv593359



Internal ID16034082
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:1870814..1872274hg38UCSC Ensembl
Innerchr4:1872541..1874001hg19UCSC Ensembl
Innerchr4:1842339..1843799hg18UCSC Ensembl
Cytoband4p16.3
Allele length
AssemblyAllele length
hg381461
hg191461
hg181461
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv8903n54
Supporting Variantsnssv988490, nssv988492, nssv988491
Samples
Known GenesWHSC1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv593359
Frequency
Sample Size17421
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


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