A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6551792



Internal ID20924925
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:17114373..17120553hg38UCSC Ensembl
chr21:18486691..18492871hg19UCSC Ensembl
Cytoband21q21.1
Allele length
AssemblyAllele length
hg386181
hg196181
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18069388
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6551792
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