A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv576811



Internal ID16364220
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:46333769..46351009hg38UCSC Ensembl
Innerchr18:43913732..43930972hg19UCSC Ensembl
Innerchr18:42167730..42184970hg18UCSC Ensembl
Cytoband18q21.1
Allele length
AssemblyAllele length
hg3817241
hg1917241
hg1817241
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv882695
Samples
Known GenesRNF165
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv576811
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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