A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6047920



Internal ID21957154
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:36388496..36388586hg38UCSC Ensembl
chr21:37760794..37760884hg19UCSC Ensembl
Cytoband21q22.12
Allele length
AssemblyAllele length
hg3891
hg1991
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17640438
Samples
Known GenesCHAF1B
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6047920
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