A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17579336



Internal ID21771379
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:118345915..118347446hg38UCSC Ensembl
chr10:120105427..120106958hg19UCSC Ensembl
Cytoband10q26.11
Allele length
AssemblyAllele length
hg381532
hg191532
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6008432
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17579336
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