A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv577091



Internal ID16364500
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:62522681..62525895hg38UCSC Ensembl
Innerchr18:60189914..60193128hg19UCSC Ensembl
Innerchr18:58340894..58344108hg18UCSC Ensembl
Cytoband18q21.33
Allele length
AssemblyAllele length
hg383215
hg193215
hg183215
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5967n54
Supporting Variantsnssv884990
Samples
Known GenesZCCHC2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv577091
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer