A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17032312



Internal ID89241
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:26595226..26929368hg38UCSC Ensembl
chr10:26884155..27218297hg19UCSC Ensembl
Cytoband10p12.1
Allele length
AssemblyAllele length
hg38334143
hg19334143
Variant TypeOTHER sequence alteration
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5560604
Supporting Variants
Samples
Known GenesABI1, LINC00202-2, PDSS1
MethodSequencing
Analysis
Platform
Commentscomplex variant
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17032312
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.001717


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