A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv884992



Internal ID16178948
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:62523666..62526204hg38UCSC Ensembl
Innerchr18:60190899..60193437hg19UCSC Ensembl
Innerchr18:58341879..58344417hg18UCSC Ensembl
Cytoband18q21.33
Allele length
AssemblyAllele length
hg382539
hg192539
hg182539
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv577093
Supporting Variants
Samples
Known GenesZCCHC2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv884992
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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