A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6602883



Internal ID20975954
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:159691901..159693800hg38UCSC Ensembl
chr6:160112933..160114832hg19UCSC Ensembl
Cytoband6q25.3
Allele length
AssemblyAllele length
hg381900
hg191900
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18142442
Samples
Known GenesSOD2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6602883
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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