A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6564128



Internal ID20937199
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:92881736..92883451hg38UCSC Ensembl
chr9:95644018..95645733hg19UCSC Ensembl
Cytoband9q22.31
Allele length
AssemblyAllele length
hg381716
hg191716
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18281456
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6564128
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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