A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14242918



Internal ID21310304
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:66867181..66907043hg38UCSC Ensembl
Outerchr18:66866438..66908584hg38UCSC Ensembl
Innerchr18:64534418..64574280hg19UCSC Ensembl
Outerchr18:64533675..64575821hg19UCSC Ensembl
Innerchr18:62685398..62725260hg18UCSC Ensembl
Outerchr18:62684655..62726801hg18UCSC Ensembl
Cytoband18q22.1
Allele length
AssemblyAllele length
hg3842147
hg1942147
hg1842147
Variant TypeCNV deletion
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3169561
Supporting Variants
SamplesNGO_6
Known Genes
MethodSNP array
Analysis
PlatformAffymetrix Genome-wide SNP array 6.0
Comments
ReferenceFu_et_al_2018
Pubmed ID29476164
Accession Number(s)nssv14242918
Frequency
Sample Size93
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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