A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14087094



Internal ID21267587
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:39484347..39503164hg38UCSC Ensembl
Innerchr8:39341866..39360683hg19UCSC Ensembl
Cytoband8p11.22
Allele length
AssemblyAllele length
hg3818818
hg1918818
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3111691
Supporting Variants
Samplessample114
Known GenesADAM3A
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14087094
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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