A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv890082



Internal ID15837352
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:79731280..79767009hg38UCSC Ensembl
Innerchr18:77491280..77527009hg19UCSC Ensembl
Innerchr18:75592268..75627997hg18UCSC Ensembl
Cytoband18q23
Allele length
AssemblyAllele length
hg3835730
hg1935730
hg1835730
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv577906
Supporting Variants
Samples
Known GenesCTDP1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv890082
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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