A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18009088



Internal ID20576130
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:43688723..43689113hg38UCSC Ensembl
chr13:44262859..44263249hg19UCSC Ensembl
Cytoband13q14.11
Allele length
AssemblyAllele length
hg38391
hg19391
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6491796
Supporting Variants
Samples
Known GenesENOX1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18009088
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00065


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