A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18014246



Internal ID20581286
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:84880189..84957420hg38UCSC Ensembl
chr13:85454324..85531555hg19UCSC Ensembl
Cytoband13q31.1
Allele length
AssemblyAllele length
hg3877232
hg1977232
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6475656
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18014246
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