A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6566170



Internal ID20939241
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:74313523..74313734hg38UCSC Ensembl
chr9:76928439..76928650hg19UCSC Ensembl
Cytoband9q21.13
Allele length
AssemblyAllele length
hg38212
hg19212
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18280961
Samples
Known GenesMIR6130
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6566170
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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