A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17989378



Internal ID20556418
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:15265101..15266000hg38UCSC Ensembl
chr11:15286647..15287546hg19UCSC Ensembl
Cytoband11p15.2
Allele length
AssemblyAllele length
hg38900
hg19900
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6447034
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv17989378
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00021


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