A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6555780



Internal ID20928851
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:96275930..96276291hg38UCSC Ensembl
chr9:99038212..99038573hg19UCSC Ensembl
Cytoband9q22.32
Allele length
AssemblyAllele length
hg38362
hg19362
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18281543
Samples
Known GenesHSD17B3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6555780
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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