A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6560651



Internal ID20933722
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:82289541..82290582hg38UCSC Ensembl
chr6:82999258..83000299hg19UCSC Ensembl
Cytoband6q14.1
Allele length
AssemblyAllele length
hg381042
hg191042
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18274763
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6560651
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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