A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6454881



Internal ID21112434
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:121937797..121943890hg38UCSC Ensembl
chr10:123697312..123703405hg19UCSC Ensembl
Cytoband10q26.13
Allele length
AssemblyAllele length
hg386094
hg196094
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17978188
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6454881
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer