A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3116881



Internal ID21300147
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:83901682..83908210hg38UCSC Ensembl
Innerchr15:84570434..84576962hg19UCSC Ensembl
Cytoband15q25.2
Allele length
AssemblyAllele length
hg386529
hg196529
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14097553
Samplessample218
Known GenesADAMTSL3
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3116881
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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