A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6564856



Internal ID20937927
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:125870312..125871308hg38UCSC Ensembl
chr9:128632591..128633587hg19UCSC Ensembl
Cytoband9q33.3
Allele length
AssemblyAllele length
hg38997
hg19997
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7937n223
Supporting Variantsnssv18279915
Samples
Known GenesPBX3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6564856
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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