A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3169397



Internal ID21313880
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 Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14244781, nssv14250352
SamplesPML_3, NGO_16
Known Genes
MethodSNP array
Analysis
PlatformAffymetrix Genome-wide SNP array 6.0
Comments
ReferenceFu_et_al_2018
Pubmed ID29476164
Accession Number(s)nsv3169397
Frequency
Sample Size93
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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