A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv883300



Internal ID16177256
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:52618163..52631750hg38UCSC Ensembl
Innerchr18:50144533..50158120hg19UCSC Ensembl
Innerchr18:48398531..48412118hg18UCSC Ensembl
Cytoband18q21.2
Allele length
AssemblyAllele length
hg3813588
hg1913588
hg1813588
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv576936
Supporting Variants
Samples
Known GenesDCC
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv883300
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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