A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18011192



Internal ID20578232
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:63183601..63184600hg38UCSC Ensembl
chr13:63757734..63758733hg19UCSC Ensembl
Cytoband13q21.31
Allele length
AssemblyAllele length
hg381000
hg191000
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6490845
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18011192
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