A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6563843



Internal ID20936914
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:86329215..86330215hg38UCSC Ensembl
chr9:88944130..88945130hg19UCSC Ensembl
Cytoband9q21.33
Allele length
AssemblyAllele length
hg381001
hg191001
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18281305
Samples
Known GenesZCCHC6
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6563843
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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