A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3115613



Internal ID21298879
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:75933883..75940531hg38UCSC Ensembl
Innerchr6:76643600..76650248hg19UCSC Ensembl
Cytoband6q14.1
Allele length
AssemblyAllele length
hg386649
hg196649
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14082841
Samplessample9
Known GenesIMPG1
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3115613
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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