A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18229742



Internal ID20796782
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:27256321..27295808hg38UCSC Ensembl
chr8:27113838..27153325hg19UCSC Ensembl
Cytoband8p21.2
Allele length
AssemblyAllele length
hg3839488
hg1939488
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6430189
Supporting Variants
Samples
Known GenesSTMN4, TRIM35
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18229742
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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