A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17977244



Internal ID20544284
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:102154928..102157716hg38UCSC Ensembl
chr10:103914685..103917473hg19UCSC Ensembl
Cytoband10q24.32
Allele length
AssemblyAllele length
hg382789
hg192789
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6440568
Supporting Variants
Samples
Known GenesNOLC1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv17977244
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