A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6562996



Internal ID20936067
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:11124816..11126075hg38UCSC Ensembl
chr8:10982326..10983585hg19UCSC Ensembl
Cytoband8p23.1
Allele length
AssemblyAllele length
hg381260
hg191260
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18276945
Samples
Known GenesXKR6
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6562996
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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