A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv887095



Internal ID16181051
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:70284647..70287810hg38UCSC Ensembl
Innerchr18:67951883..67955046hg19UCSC Ensembl
Innerchr18:66102863..66106026hg18UCSC Ensembl
Cytoband18q22.2
Allele length
AssemblyAllele length
hg383164
hg193164
hg183164
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv577550
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv887095
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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