A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv577590



Internal ID16364999
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:71340793..71380915hg38UCSC Ensembl
Innerchr18:69008029..69048151hg19UCSC Ensembl
Innerchr18:67159009..67199131hg18UCSC Ensembl
Cytoband18q22.3
Allele length
AssemblyAllele length
hg3840123
hg1940123
hg1840123
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6063n54
Supporting Variantsnssv887253
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv577590
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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