A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14248717



Internal ID21310603
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:142021378..142033732hg38UCSC Ensembl
Outerchr8:142019056..142036153hg38UCSC Ensembl
Innerchr8:143102739..143115093hg19UCSC Ensembl
Outerchr8:143100417..143117514hg19UCSC Ensembl
Innerchr8:143100646..143113000hg18UCSC Ensembl
Outerchr8:143098324..143115421hg18UCSC Ensembl
Cytoband8q24.3
Allele length
AssemblyAllele length
hg3817098
hg1917098
hg1817098
Variant TypeCNV deletion
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3170064
Supporting Variants
SamplesNGO_9
Known Genes
MethodSNP array
Analysis
PlatformAffymetrix Genome-wide SNP array 6.0
Comments
ReferenceFu_et_al_2018
Pubmed ID29476164
Accession Number(s)nssv14248717
Frequency
Sample Size93
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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