A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6571456



Internal ID20944527
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:91353398..91353586hg38UCSC Ensembl
chr9:94115680..94115868hg19UCSC Ensembl
Cytoband9q22.31
Allele length
AssemblyAllele length
hg38189
hg19189
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18281400
Samples
Known GenesAUH
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6571456
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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