A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1056964



Internal ID19146183
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:71301821..71382241hg38UCSC Ensembl
Innerchr18:68969057..69049477hg19UCSC Ensembl
Innerchr18:67120037..67200457hg18UCSC Ensembl
Cytoband18q22.3
Allele length
AssemblyAllele length
hg3880421
hg1980421
hg1880421
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3562968
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1056964
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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