A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5540569



Internal ID315314
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:33512682..33516777hg38UCSC Ensembl
chr21:34884989..34889084hg19UCSC Ensembl
Cytoband21q22.11
Allele length
AssemblyAllele length
hg384096
hg194096
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17726667
Samples
Known GenesGART
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5540569
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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