A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17517782



Internal ID21842141
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:86937993..87015660hg38UCSC Ensembl
chr1:87403676..87481343hg19UCSC Ensembl
Cytoband1p22.3
Allele length
AssemblyAllele length
hg3877668
hg1977668
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5985015
Supporting Variants
Samples
Known GenesHS2ST1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17517782
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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