A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6559816



Internal ID20932887
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:73511690..73512027hg38UCSC Ensembl
chr9:76126606..76126943hg19UCSC Ensembl
Cytoband9q21.13
Allele length
AssemblyAllele length
hg38338
hg19338
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18280948
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6559816
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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