A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6605539



Internal ID20978610
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:159653701..159728800hg38UCSC Ensembl
chr6:160074733..160149832hg19UCSC Ensembl
Cytoband6q25.3
Allele length
AssemblyAllele length
hg3875100
hg1975100
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18216720
Samples
Known GenesSOD2, WTAP
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6605539
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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