A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6559894



Internal ID20932965
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:125311090..125311453hg38UCSC Ensembl
chr9:128073369..128073732hg19UCSC Ensembl
Cytoband9q33.3
Allele length
AssemblyAllele length
hg38364
hg19364
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18279887
Samples
Known GenesGAPVD1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6559894
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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