A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5985015



Internal ID21894358
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 StatusM
Merged Variants
Supporting Variantsnssv17517782
Samples
Known GenesHS2ST1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv5985015
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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