A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14242197



Internal ID21306836
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:142018623..142033256hg38UCSC Ensembl
Outerchr8:142016479..142033732hg38UCSC Ensembl
Innerchr8:143099984..143114617hg19UCSC Ensembl
Outerchr8:143097840..143115093hg19UCSC Ensembl
Innerchr8:143097891..143112524hg18UCSC Ensembl
Outerchr8:143095747..143113000hg18UCSC Ensembl
Cytoband8q24.3
Allele length
AssemblyAllele length
hg3817254
hg1917254
hg1817254
Variant TypeCNV deletion
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3170064
Supporting Variants
SamplesNGO_30
Known Genes
MethodSNP array
Analysis
PlatformAffymetrix Genome-wide SNP array 6.0
Comments
ReferenceFu_et_al_2018
Pubmed ID29476164
Accession Number(s)nssv14242197
Frequency
Sample Size93
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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