A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1059918



Internal ID19149137
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:71227555..71340217hg38UCSC Ensembl
Innerchr18:68894791..69007453hg19UCSC Ensembl
Innerchr18:67045771..67158433hg18UCSC Ensembl
Cytoband18q22.3
Allele length
AssemblyAllele length
hg38112663
hg19112663
hg18112663
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3562967
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)nsv1059918
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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