A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3113994



Internal ID21297260
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:39375767..39465829hg38UCSC Ensembl
Innerchr8:39233286..39323348hg19UCSC Ensembl
Cytoband8p11.22
Allele length
AssemblyAllele length
hg3890063
hg1990063
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1173n145
Supporting Variantsnssv14088191
Samplessample374
Known GenesADAM3A, ADAM5
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3113994
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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