A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6551350



Internal ID20924486
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:19279335..19279681hg38UCSC Ensembl
chr21:20651652..20651998hg19UCSC Ensembl
Cytoband21q21.1
Allele length
AssemblyAllele length
hg38347
hg19347
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18070751
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6551350
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