A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6550269



Internal ID20923418
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:36594944..36625681hg38UCSC Ensembl
chr21:37967242..37997979hg19UCSC Ensembl
Cytoband21q22.13
Allele length
AssemblyAllele length
hg3830738
hg1930738
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18072213
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6550269
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