A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6574989



Internal ID20948060
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:65654038..65654257hg38UCSC Ensembl
chr8:66566273..66566492hg19UCSC Ensembl
Cytoband8q13.1
Allele length
AssemblyAllele length
hg38220
hg19220
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18278457
Samples
Known GenesMTFR1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6574989
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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