A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6018675



Internal ID21928018
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:96941372..96941747hg38UCSC Ensembl
chr10:98701129..98701504hg19UCSC Ensembl
Cytoband10q24.1
Allele length
AssemblyAllele length
hg38376
hg19376
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17595013
Samples
Known GenesLCOR
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6018675
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