A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17558553



Internal ID21882908
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:1297838..1298045hg38UCSC Ensembl
chr8:1246138..1246301hg19UCSC Ensembl
Cytoband8p23.3
Allele length
AssemblyAllele length
hg38208
hg19164
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6016843
Supporting Variants
Samples
Known GenesLOC286083
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17558553
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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