A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17590385



Internal ID21782428
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:90631705..90645111hg38UCSC Ensembl
chr8:91643933..91657339hg19UCSC Ensembl
Cytoband8q21.3
Allele length
AssemblyAllele length
hg3813407
hg1913407
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6018828
Supporting Variants
Samples
Known GenesTMEM64
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17590385
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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