A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6569300



Internal ID20942371
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:125166713..125167417hg38UCSC Ensembl
chr9:127928992..127929696hg19UCSC Ensembl
Cytoband9q33.3
Allele length
AssemblyAllele length
hg38705
hg19705
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18279868
Samples
Known GenesPPP6C
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6569300
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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