A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv884984



Internal ID15832254
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:62522582..62524730hg38UCSC Ensembl
Innerchr18:60189815..60191963hg19UCSC Ensembl
Innerchr18:58340795..58342943hg18UCSC Ensembl
Cytoband18q21.33
Allele length
AssemblyAllele length
hg382149
hg192149
hg182149
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv577087
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)nssv884984
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