A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17726397



Internal ID150063
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:26123905..26123999hg38UCSC Ensembl
chr21:27496222..27496316hg19UCSC Ensembl
Cytoband21q21.3
Allele length
AssemblyAllele length
hg3895
hg1995
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5522054
Supporting Variants
Samples
Known GenesAPP
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17726397
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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