A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv884940



Internal ID16178896
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:62039466..62040090hg38UCSC Ensembl
Innerchr18:59706699..59707323hg19UCSC Ensembl
Innerchr18:57857679..57858303hg18UCSC Ensembl
Cytoband18q21.33
Allele length
AssemblyAllele length
hg38625
hg19625
hg18625
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv577075
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv884940
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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