A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14086277



Internal ID21278675
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:57592030..57596049hg38UCSC Ensembl
Innerchr8:58504589..58508608hg19UCSC Ensembl
Cytoband8q12.1
Allele length
AssemblyAllele length
hg384020
hg194020
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3111447
Supporting Variants
Samplessample272
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14086277
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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