A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv988456



Internal ID15935726
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:1870601..1872274hg38UCSC Ensembl
Innerchr4:1872328..1874001hg19UCSC Ensembl
Innerchr4:1842126..1843799hg18UCSC Ensembl
Cytoband4p16.3
Allele length
AssemblyAllele length
hg381674
hg191674
hg181674
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv593344
Supporting Variants
Samples
Known GenesWHSC1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv988456
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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