A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17584940



Internal ID21776983
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:73743768..73745468hg38UCSC Ensembl
chr8:74656003..74657703hg19UCSC Ensembl
Cytoband8q21.11
Allele length
AssemblyAllele length
hg381701
hg191701
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6016570
Supporting Variants
Samples
Known GenesSTAU2
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17584940
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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