A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17402725



Internal ID22460595
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:26145546..26150109hg38UCSC Ensembl
chr21:27517864..27522427hg19UCSC Ensembl
Cytoband21q21.3
Allele length
AssemblyAllele length
hg384564
hg194564
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5954632
Supporting Variants
Samples
Known GenesAPP
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17402725
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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