A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6567174



Internal ID20940245
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:70643304..70710569hg38UCSC Ensembl
chr8:71555539..71622804hg19UCSC Ensembl
Cytoband8q13.3
Allele length
AssemblyAllele length
hg3867266
hg1967266
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18278636
Samples
Known GenesLACTB2, LOC286190, XKR9
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6567174
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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