A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14088193



Internal ID21285455
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:39484645..39528445hg38UCSC Ensembl
Innerchr8:39342164..39385964hg19UCSC Ensembl
Cytoband8p11.22
Allele length
AssemblyAllele length
hg3843801
hg1943801
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3115960
Supporting Variants
Samplessample374
Known GenesADAM3A
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14088193
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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