A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6015131



Internal ID21924474
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:78468525..78468752hg38UCSC Ensembl
chr10:80228282..80228509hg19UCSC Ensembl
Cytoband10q22.3
Allele length
AssemblyAllele length
hg38228
hg19228
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17591110
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6015131
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