A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17032388



Internal ID89289
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:9186120..9189237hg38UCSC Ensembl
chr10:9228083..9231200hg19UCSC Ensembl
Cytoband10p14
Allele length
AssemblyAllele length
hg383118
hg193118
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5488629
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17032388
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000624


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