A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18008943



Internal ID20575985
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:41325019..41329560hg38UCSC Ensembl
chr13:41899155..41903696hg19UCSC Ensembl
Cytoband13q14.11
Allele length
AssemblyAllele length
hg384542
hg194542
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6492885
Supporting Variants
Samples
Known GenesNAA16
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18008943
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