A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv576635



Internal ID16017358
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:31549968..31568851hg38UCSC Ensembl
Innerchr18:29129931..29148814hg19UCSC Ensembl
Innerchr18:27383929..27402812hg18UCSC Ensembl
Cytoband18q12.1
Allele length
AssemblyAllele length
hg3818884
hg1918884
hg1818884
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv878944
Samples
Known GenesLOC100652770
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv576635
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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