A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6574219



Internal ID20947290
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:107373003..107374273hg38UCSC Ensembl
chr6:107694207..107695477hg19UCSC Ensembl
Cytoband6q21
Allele length
AssemblyAllele length
hg381271
hg191271
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18270403
Samples
Known GenesPDSS2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6574219
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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