A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3116108



Internal ID21299374
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:82042625..82049064hg38UCSC Ensembl
Innerchr15:82334966..82341405hg19UCSC Ensembl
Cytoband15q25.2
Allele length
AssemblyAllele length
hg386440
hg196440
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv411n145
Supporting Variantsnssv14097203
Samplessample363
Known GenesMEX3B
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3116108
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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