A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6561182



Internal ID20934253
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:125834398..125835020hg38UCSC Ensembl
chr9:128596677..128597299hg19UCSC Ensembl
Cytoband9q33.3
Allele length
AssemblyAllele length
hg38623
hg19623
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18279911
Samples
Known GenesPBX3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6561182
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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