A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17588679



Internal ID21780722
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:120798394..120798510hg38UCSC Ensembl
chr10:122557906..122558022hg19UCSC Ensembl
Cytoband10q26.12
Allele length
AssemblyAllele length
hg38117
hg19117
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6006977
Supporting Variants
Samples
Known GenesMIR5694, WDR11-AS1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17588679
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