A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6562752



Internal ID20935823
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:86051014..86393052hg38UCSC Ensembl
chr9:88665929..89007967hg19UCSC Ensembl
Cytoband9q21.33
Allele length
AssemblyAllele length
hg38342039
hg19342039
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7865n223
Supporting Variantsnssv18281293
Samples
Known GenesC9orf153, GOLM1, ISCA1, ZCCHC6
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6562752
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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