A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6015488



Internal ID21924831
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:114583441..114583496hg38UCSC Ensembl
chr10:116343200..116343255hg19UCSC Ensembl
Cytoband10q25.3
Allele length
AssemblyAllele length
hg3856
hg1956
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17593950
Samples
Known GenesABLIM1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6015488
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