A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv878077



Internal ID15825347
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:9913348..9926905hg38UCSC Ensembl
Innerchr18:9913345..9926902hg19UCSC Ensembl
Innerchr18:9903345..9916902hg18UCSC Ensembl
Cytoband18p11.22
Allele length
AssemblyAllele length
hg3813558
hg1913558
hg1813558
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv576456
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)nssv878077
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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