A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18013363



Internal ID20580403
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:75578201..75580500hg38UCSC Ensembl
chr13:76152337..76154636hg19UCSC Ensembl
Cytoband13q22.2
Allele length
AssemblyAllele length
hg382300
hg192300
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6479005
Supporting Variants
Samples
Known GenesUCHL3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18013363
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00013


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