A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18221468



Internal ID20788508
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:93469801..93486719hg38UCSC Ensembl
chr8:94482029..94498947hg19UCSC Ensembl
Cytoband8q22.1
Allele length
AssemblyAllele length
hg3816919
hg1916919
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6433186
Supporting Variants
Samples
Known GenesLINC00535
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18221468
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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