A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6571813



Internal ID20944884
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:85927474..86736192hg38UCSC Ensembl
chr6:86637192..87445910hg19UCSC Ensembl
Cytoband6q14.3
Allele length
AssemblyAllele length
hg38808719
hg19808719
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18274836
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6571813
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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