A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5530833



Internal ID306803
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:6374502..6374995hg38UCSC Ensembl
chr17_gl000205_random:89982..90445hg19UCSC Ensembl
Cytoband
Allele length
AssemblyAllele length
hg38494
hg19464
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17733796
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5530833
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer