A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6563111



Internal ID20936182
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:10214927..10216153hg38UCSC Ensembl
chr8:10072437..10073663hg19UCSC Ensembl
Cytoband8p23.1
Allele length
AssemblyAllele length
hg381227
hg191227
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18275923
Samples
Known GenesMSRA
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6563111
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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