A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5532652



Internal ID308568
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:25808274..25875166hg38UCSC Ensembl
chr21:27180585..27247477hg19UCSC Ensembl
Cytoband21q21.3
Allele length
AssemblyAllele length
hg3866893
hg1966893
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17726380
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5532652
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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