A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv884961



Internal ID16178917
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:62039493..62040192hg38UCSC Ensembl
Innerchr18:59706726..59707425hg19UCSC Ensembl
Innerchr18:57857706..57858405hg18UCSC Ensembl
Cytoband18q21.33
Allele length
AssemblyAllele length
hg38700
hg19700
hg18700
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv577081
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)nssv884961
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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