A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17733859



Internal ID157525
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:9038252..9195900hg38UCSC Ensembl
chr21:9877085..10034733hg19UCSC Ensembl
Cytoband21p11.2
Allele length
AssemblyAllele length
hg38157649
hg19157649
Variant TypeOTHER copy number variation
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5415421
Supporting Variants
Samples
Known GenesTEKT4P2
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17733859
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.163849


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