A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6479005



Internal ID21136558
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 StatusM
Merged Variants
Supporting Variantsnssv18013363
Samples
Known GenesUCHL3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6479005
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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