A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14248102



Internal ID21312755
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:142021378..142033256hg38UCSC Ensembl
Outerchr8:142019056..142033732hg38UCSC Ensembl
Innerchr8:143102739..143114617hg19UCSC Ensembl
Outerchr8:143100417..143115093hg19UCSC Ensembl
Innerchr8:143100646..143112524hg18UCSC Ensembl
Outerchr8:143098324..143113000hg18UCSC Ensembl
Cytoband8q24.3
Allele length
AssemblyAllele length
hg3814677
hg1914677
hg1814677
Variant TypeCNV deletion
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3170064
Supporting Variants
SamplesSNI_4
Known Genes
MethodSNP array
Analysis
PlatformAffymetrix Genome-wide SNP array 6.0
Comments
ReferenceFu_et_al_2018
Pubmed ID29476164
Accession Number(s)nssv14248102
Frequency
Sample Size93
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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