A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6569355



Internal ID20942426
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:108298379..108299126hg38UCSC Ensembl
chr6:108619583..108620330hg19UCSC Ensembl
Cytoband6q21
Allele length
AssemblyAllele length
hg38748
hg19748
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18267784
Samples
Known GenesLACE1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6569355
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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