A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3117105



Internal ID21300371
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:39483102..39499344hg38UCSC Ensembl
Innerchr8:39340621..39356863hg19UCSC Ensembl
Cytoband8p11.22
Allele length
AssemblyAllele length
hg3816243
hg1916243
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1177n145
Supporting Variantsnssv14087410
Samplessample326
Known GenesADAM3A
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3117105
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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