A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3169561



Internal ID21313794
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:66866438..66907043hg38UCSC Ensembl
Outerchr18:66863456..66908584hg38UCSC Ensembl
Innerchr18:64533675..64574280hg19UCSC Ensembl
Outerchr18:64530693..64575821hg19UCSC Ensembl
Innerchr18:62684655..62725260hg18UCSC Ensembl
Outerchr18:62681673..62726801hg18UCSC Ensembl
Cytoband18q22.1
Allele length
AssemblyAllele length
hg3845129
hg1945129
hg1845129
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14246451, nssv14252044, nssv14252524, nssv14243446, nssv14242918
SamplesNGO_6, SNI_3, SNI_6, NGO_7, NGO_51
Known Genes
MethodSNP array
Analysis
PlatformAffymetrix Genome-wide SNP array 6.0
Comments
ReferenceFu_et_al_2018
Pubmed ID29476164
Accession Number(s)nsv3169561
Frequency
Sample Size93
Observed Gain0
Observed Loss5
Observed Complex0
Frequencyn/a


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