A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17588985



Internal ID21781028
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:73315190..73315190hg38UCSC Ensembl
chr8:74227425..74227425hg19UCSC Ensembl
Cytoband8q21.11
Allele length
AssemblyAllele length
hg3880
hg1980
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6065170
Supporting Variants
Samples
Known GenesRDH10
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17588985
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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