A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17576927



Internal ID21768970
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:20127071..20168884hg38UCSC Ensembl
chr8:19984582..20026395hg19UCSC Ensembl
Cytoband8p21.3
Allele length
AssemblyAllele length
hg3841814
hg1941814
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6011191
Supporting Variants
Samples
Known GenesSLC18A1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17576927
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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