A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17734082



Internal ID157748
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:14932404..14937808hg38UCSC Ensembl
chr21:16304725..16310129hg19UCSC Ensembl
Cytoband21q11.2
Allele length
AssemblyAllele length
hg385405
hg195405
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5529725
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17734082
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000312


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