A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14252044



Internal ID21312919
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:66873245..66907043hg38UCSC Ensembl
Outerchr18:66869237..66908584hg38UCSC Ensembl
Innerchr18:64540482..64574280hg19UCSC Ensembl
Outerchr18:64536474..64575821hg19UCSC Ensembl
Innerchr18:62691462..62725260hg18UCSC Ensembl
Outerchr18:62687454..62726801hg18UCSC Ensembl
Cytoband18q22.1
Allele length
AssemblyAllele length
hg3839348
hg1939348
hg1839348
Variant TypeCNV deletion
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3169561
Supporting Variants
SamplesSNI_6
Known Genes
MethodSNP array
Analysis
PlatformAffymetrix Genome-wide SNP array 6.0
Comments
ReferenceFu_et_al_2018
Pubmed ID29476164
Accession Number(s)nssv14252044
Frequency
Sample Size93
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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