A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv887376



Internal ID16181332
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:74139133..74188803hg38UCSC Ensembl
Innerchr18:71806368..71856038hg19UCSC Ensembl
Innerchr18:69957348..70007018hg18UCSC Ensembl
Cytoband18q22.3
Allele length
AssemblyAllele length
hg3849671
hg1949671
hg1849671
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv577650
Supporting Variants
Samples
Known GenesFBXO15, TIMM21
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv887376
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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