A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3114569



Internal ID21297835
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:82042625..82047837hg38UCSC Ensembl
Innerchr15:82334966..82340178hg19UCSC Ensembl
Cytoband15q25.2
Allele length
AssemblyAllele length
hg385213
hg195213
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv411n145
Supporting Variantsnssv14096100
Samplessample116
Known GenesMEX3B
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3114569
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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