A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17726805



Internal ID150471
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:36952431..36952738hg38UCSC Ensembl
chr21:38324731..38325038hg19UCSC Ensembl
Cytoband21q22.13
Allele length
AssemblyAllele length
hg38308
hg19308
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5541580
Supporting Variants
Samples
Known GenesHLCS
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17726805
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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