A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17596800



Internal ID21788843
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:90233242..90233242hg38UCSC Ensembl
chr8:91245470..91245470hg19UCSC Ensembl
Cytoband8q21.3
Allele length
AssemblyAllele length
hg3855
hg1955
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6074125
Supporting Variants
Samples
Known GenesLINC00534
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17596800
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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