A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6567674



Internal ID20940745
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:94205001..94206613hg38UCSC Ensembl
chr9:96967283..96968895hg19UCSC Ensembl
Cytoband9q22.32
Allele length
AssemblyAllele length
hg381613
hg191613
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18281485
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6567674
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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