A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6014669



Internal ID21924012
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:101728971..101731073hg38UCSC Ensembl
chr10:103488728..103490830hg19UCSC Ensembl
Cytoband10q24.32
Allele length
AssemblyAllele length
hg382103
hg192103
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17586040
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6014669
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