A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16911461



Internal ID8403
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:37170982..37171930hg38UCSC Ensembl
chr2:37398125..37399073hg19UCSC Ensembl
Cytoband2p22.2
Allele length
AssemblyAllele length
hg38949
hg19949
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5438523
Supporting Variants
Samples
Known GenesSULT6B1
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16911461
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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