A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv884946



Internal ID16178902
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:62039466..62040252hg38UCSC Ensembl
Innerchr18:59706699..59707485hg19UCSC Ensembl
Innerchr18:57857679..57858465hg18UCSC Ensembl
Cytoband18q21.33
Allele length
AssemblyAllele length
hg38787
hg19787
hg18787
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv577077
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)nssv884946
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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