A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5525996



Internal ID302142
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:9170328..9180604hg38UCSC Ensembl
chr21:10009161..10019437hg19UCSC Ensembl
Cytoband21p11.2
Allele length
AssemblyAllele length
hg3810277
hg1910277
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17733863
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5525996
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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