A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv2795068



Internal ID21240406
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 StatusM
Merged Variants
Supporting Variantsnssv13688522
Samples
Known GenesPPP1R14D
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nsv2795068
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer