A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv988482



Internal ID15935752
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:1870705..1872507hg38UCSC Ensembl
Innerchr4:1872432..1874234hg19UCSC Ensembl
Innerchr4:1842230..1844032hg18UCSC Ensembl
Cytoband4p16.3
Allele length
AssemblyAllele length
hg381803
hg191803
hg181803
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv593354
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)nssv988482
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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