A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3117349



Internal ID21300615
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:76929850..76933763hg38UCSC Ensembl
Innerchr15:77222191..77226104hg19UCSC Ensembl
Cytoband15q24.3
Allele length
AssemblyAllele length
hg383914
hg193914
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14097174, nssv14097178
Samplessample349, sample348
Known GenesRCN2
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3117349
Frequency
Sample Size467
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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