A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3117794



Internal ID21301060
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:78857457..78866082hg38UCSC Ensembl
Innerchr15:79149799..79158424hg19UCSC Ensembl
Cytoband15q25.1
Allele length
AssemblyAllele length
hg388626
hg198626
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14095977, nssv14097560
Samplessample222, sample43
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3117794
Frequency
Sample Size467
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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