A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6563547



Internal ID20936618
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:25386534..25387121hg38UCSC Ensembl
chr6:25386762..25387349hg19UCSC Ensembl
Cytoband6p22.2
Allele length
AssemblyAllele length
hg38588
hg19588
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18270896
Samples
Known GenesLRRC16A
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6563547
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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