A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17594986



Internal ID21787029
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:73847166..73866872hg38UCSC Ensembl
chr8:74759401..74779107hg19UCSC Ensembl
Cytoband8q21.11
Allele length
AssemblyAllele length
hg3819707
hg1919707
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6000478
Supporting Variants
Samples
Known GenesUBE2W
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17594986
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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