A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3110890



Internal ID21294156
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:34209118..34211580hg38UCSC Ensembl
Innerchr15:34501319..34503781hg19UCSC Ensembl
Cytoband15q14
Allele length
AssemblyAllele length
hg382463
hg192463
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14097562
Samplessample224
Known GenesKATNBL1
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3110890
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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