A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6454845



Internal ID21112398
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:84705122..84705803hg38UCSC Ensembl
chr10:86464878..86465559hg19UCSC Ensembl
Cytoband10q23.1
Allele length
AssemblyAllele length
hg38682
hg19682
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17984614
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6454845
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