A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6564031



Internal ID20937102
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:128184685..128185150hg38UCSC Ensembl
chr9:130946964..130947429hg19UCSC Ensembl
Cytoband9q34.11
Allele length
AssemblyAllele length
hg38466
hg19466
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7945n223
Supporting Variantsnssv18279970
Samples
Known GenesCIZ1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6564031
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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