A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv878099



Internal ID15825369
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:9913909..9925703hg38UCSC Ensembl
Innerchr18:9913906..9925700hg19UCSC Ensembl
Innerchr18:9903906..9915700hg18UCSC Ensembl
Cytoband18p11.22
Allele length
AssemblyAllele length
hg3811795
hg1911795
hg1811795
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv576463
Supporting Variants
Samples
Known GenesVAPA
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv878099
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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