A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv883089



Internal ID15830359
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:50227099..50287465hg38UCSC Ensembl
Innerchr18:47753469..47813835hg19UCSC Ensembl
Innerchr18:46007467..46067833hg18UCSC Ensembl
Cytoband18q21.1
Allele length
AssemblyAllele length
hg3860367
hg1960367
hg1860367
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv576889
Supporting Variants
Samples
Known GenesCCDC11, CXXC1, MBD1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv883089
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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