A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3112436



Internal ID21295702
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:39375767..39530975hg38UCSC Ensembl
Innerchr8:39233286..39388494hg19UCSC Ensembl
Cytoband8p11.22
Allele length
AssemblyAllele length
hg38155209
hg19155209
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1171n145
Supporting Variantsnssv14086983
Samplessample87
Known GenesADAM3A, ADAM5
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3112436
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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