A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6567285



Internal ID20940356
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:97240029..97240487hg38UCSC Ensembl
chr9:100002311..100002769hg19UCSC Ensembl
Cytoband9q22.33
Allele length
AssemblyAllele length
hg38459
hg19459
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18281575
Samples
Known GenesLOC100499484, LOC100499484-C9ORF174
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6567285
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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