A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3110925



Internal ID21294191
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:39375671..39454268hg38UCSC Ensembl
Innerchr8:39233190..39311787hg19UCSC Ensembl
Cytoband8p11.22
Allele length
AssemblyAllele length
hg3878598
hg1978598
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1173n145
Supporting Variantsnssv14086952
Samplessample79
Known GenesADAM3A, ADAM5
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3110925
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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