A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17030912



Internal ID88320
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:1045321..1045333hg38UCSC Ensembl
chr10:1091261..1091273hg19UCSC Ensembl
Cytoband10p15.3
Allele length
AssemblyAllele length
hg3859
hg1959
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5544580
Supporting Variants
Samples
Known GenesIDI1
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17030912
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000781


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