A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv577094



Internal ID16364503
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:62523954..62526204hg38UCSC Ensembl
Innerchr18:60191187..60193437hg19UCSC Ensembl
Innerchr18:58342167..58344417hg18UCSC Ensembl
Cytoband18q21.33
Allele length
AssemblyAllele length
hg382251
hg192251
hg182251
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5968n54
Supporting Variantsnssv884993
Samples
Known GenesZCCHC2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv577094
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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