A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6559366



Internal ID20932437
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:34302176..34302642hg38UCSC Ensembl
chr6:34269953..34270419hg19UCSC Ensembl
Cytoband6p21.31
Allele length
AssemblyAllele length
hg38467
hg19467
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18271226
Samples
Known GenesNUDT3, RPS10-NUDT3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6559366
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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