A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6559721



Internal ID20932792
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:100058280..100059501hg38UCSC Ensembl
chr9:102820562..102821783hg19UCSC Ensembl
Cytoband9q31.1
Allele length
AssemblyAllele length
hg381222
hg191222
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18279297
Samples
Known GenesERP44
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6559721
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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