A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18229591



Internal ID20796631
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:85476006..85477333hg38UCSC Ensembl
chr6:86185724..86187051hg19UCSC Ensembl
Cytoband6q14.3
Allele length
AssemblyAllele length
hg381328
hg191328
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6400544
Supporting Variants
Samples
Known GenesNT5E
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18229591
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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