A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17726498



Internal ID150164
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:28956724..28963432hg38UCSC Ensembl
chr21:30329046..30335754hg19UCSC Ensembl
Cytoband21q21.3
Allele length
AssemblyAllele length
hg386709
hg196709
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5551214
Supporting Variants
Samples
Known GenesLTN1
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17726498
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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