A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv878941



Internal ID15826211
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:31389081..31471714hg38UCSC Ensembl
Innerchr18:28969044..29051677hg19UCSC Ensembl
Innerchr18:27223042..27305675hg18UCSC Ensembl
Cytoband18q12.1
Allele length
AssemblyAllele length
hg3882634
hg1982634
hg1882634
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv576631
Supporting Variants
Samples
Known GenesDSG3, DSG4
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv878941
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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