A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17032597



Internal ID89421
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:18712745..18772505hg38UCSC Ensembl
chr10:19001674..19061434hg19UCSC Ensembl
Cytoband10p12.31
Allele length
AssemblyAllele length
hg3859761
hg1959761
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5484441
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17032597
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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