A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv577579



Internal ID16018302
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:70287070..70293168hg38UCSC Ensembl
Innerchr18:67954306..67960404hg19UCSC Ensembl
Innerchr18:66105286..66111384hg18UCSC Ensembl
Cytoband18q22.2
Allele length
AssemblyAllele length
hg386099
hg196099
hg186099
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6061n54
Supporting Variantsnssv887241
Samples
Known GenesSOCS6
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv577579
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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