A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17734693



Internal ID158359
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:32306337..32306523hg38UCSC Ensembl
chr21:33678648..33678834hg19UCSC Ensembl
Cytoband21q22.11
Allele length
AssemblyAllele length
hg38187
hg19187
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5534253
Supporting Variants
Samples
Known GenesMRAP
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17734693
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000468


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