A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17589337



Internal ID21781380
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:121034222..121034324hg38UCSC Ensembl
chr10:122793735..122793837hg19UCSC Ensembl
Cytoband10q26.12
Allele length
AssemblyAllele length
hg38103
hg19103
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6010128
Supporting Variants
Samples
Known GenesMIR5694
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17589337
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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