A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv13688522



Internal ID21210378
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:40819377..40821755hg38UCSC Ensembl
chr15:41111575..41113953hg19UCSC Ensembl
Cytoband15q15.1
Allele length
AssemblyAllele length
hg382379
hg192379
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv2795068
Supporting Variants
Samples
Known GenesPPP1R14D
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nssv13688522
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.03125


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