A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17035747



Internal ID91577
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:52907014..53336622hg38UCSC Ensembl
chr10:54666774..55096382hg19UCSC Ensembl
Cytoband10q21.1
Allele length
AssemblyAllele length
hg38429609
hg19429609
Variant TypeOTHER sequence alteration
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5554440
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Commentscomplex variant
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17035747
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.000312


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