A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3112847



Internal ID21296113
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:43596641..43720944hg38UCSC Ensembl
Innerchr15:43888839..44013142hg19UCSC Ensembl
Cytoband15q15.3
Allele length
AssemblyAllele length
hg38124304
hg19124304
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14097157
Samplessample339
Known GenesCATSPER2, CKMT1A, CKMT1B, RNU6-28P, STRC
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3112847
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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