A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv577326



Internal ID16364735
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:67942742..68100080hg38UCSC Ensembl
Innerchr18:65609979..65767317hg19UCSC Ensembl
Innerchr18:63760959..63918297hg18UCSC Ensembl
Cytoband18q22.1
Allele length
AssemblyAllele length
hg38157339
hg19157339
hg18157339
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6012n54
Supporting Variantsnssv886399
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv577326
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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