A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv988460



Internal ID15935730
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:1870601..1891901hg38UCSC Ensembl
Innerchr4:1872328..1893628hg19UCSC Ensembl
Innerchr4:1842126..1863426hg18UCSC Ensembl
Cytoband4p16.3
Allele length
AssemblyAllele length
hg3821301
hg1921301
hg1821301
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv593346
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)nssv988460
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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