A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18027488



Internal ID20594528
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:97874083..97879487hg38UCSC Ensembl
chr15:98417313..98422717hg19UCSC Ensembl
Cytoband15q26.2
Allele length
AssemblyAllele length
hg385405
hg195405
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6497650
Supporting Variants
Samples
Known GenesLINC00923
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18027488
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