A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14095977



Internal ID21289071
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 StatusS
Merged Variantsnsv3117794
Supporting Variants
Samplessample43
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14095977
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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