A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6567402



Internal ID20940473
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:55747150..55747592hg38UCSC Ensembl
chr8:56659709..56660151hg19UCSC Ensembl
Cytoband8q12.1
Allele length
AssemblyAllele length
hg38443
hg19443
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18278273
Samples
Known GenesTMEM68
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6567402
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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