A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18044292



Internal ID20611332
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:10296201..10296900hg38UCSC Ensembl
chr19:10406877..10407576hg19UCSC Ensembl
Cytoband19p13.2
Allele length
AssemblyAllele length
hg38700
hg19700
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6520559
Supporting Variants
Samples
Known GenesICAM5
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18044292
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.07174


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer