A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv878966



Internal ID15826236
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:37461933..37487164hg38UCSC Ensembl
Innerchr18:35041896..35067127hg19UCSC Ensembl
Innerchr18:33295894..33321125hg18UCSC Ensembl
Cytoband18q12.2
Allele length
AssemblyAllele length
hg3825232
hg1925232
hg1825232
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv576658
Supporting Variants
Samples
Known GenesCELF4
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv878966
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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