A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18024518



Internal ID20591558
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:40352069..40352747hg38UCSC Ensembl
chr15:40644270..40644948hg19UCSC Ensembl
Cytoband15q15.1
Allele length
AssemblyAllele length
hg38679
hg19679
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6498869
Supporting Variants
Samples
Known GenesPHGR1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18024518
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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