A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5536090



Internal ID311646
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:36388481..36388586hg38UCSC Ensembl
chr21:37760779..37760884hg19UCSC Ensembl
Cytoband21q22.12
Allele length
AssemblyAllele length
hg38106
hg19106
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17726778
Samples
Known GenesCHAF1B
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5536090
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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