A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14244781



Internal ID21311014
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:141768716..141909214hg38UCSC Ensembl
Outerchr8:141765842..141912443hg38UCSC Ensembl
Innerchr8:142850077..142990575hg19UCSC Ensembl
Outerchr8:142847203..142993804hg19UCSC Ensembl
Innerchr8:142847984..142988482hg18UCSC Ensembl
Outerchr8:142845110..142991711hg18UCSC Ensembl
Cytoband8q24.3
Allele length
AssemblyAllele length
hg38146602
hg19146602
hg18146602
Variant TypeCNV deletion
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3169397
Supporting Variants
SamplesPML_3
Known Genes
MethodSNP array
Analysis
PlatformAffymetrix Genome-wide SNP array 6.0
Comments
ReferenceFu_et_al_2018
Pubmed ID29476164
Accession Number(s)nssv14244781
Frequency
Sample Size93
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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