A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5522532



Internal ID298797
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:28618000..28647000hg38UCSC Ensembl
chr16:28629321..28658321hg19UCSC Ensembl
Cytoband16p11.2
Allele length
AssemblyAllele length
hg3829001
hg1929001
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17707264
Samples
Known GenesSULT1A1
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5522532
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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