A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18045091



Internal ID20612131
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:18307797..18307947hg38UCSC Ensembl
chr19:18418607..18418757hg19UCSC Ensembl
Cytoband19p13.11
Allele length
AssemblyAllele length
hg38151
hg19151
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6516958
Supporting Variants
Samples
Known GenesLSM4
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18045091
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