A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6561296



Internal ID20934367
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:77409630..77482981hg38UCSC Ensembl
chr9:80024546..80097897hg19UCSC Ensembl
Cytoband9q21.2
Allele length
AssemblyAllele length
hg3873352
hg1973352
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18281070
Samples
Known GenesGNA14, VPS13A
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6561296
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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