A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6561034



Internal ID20934105
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:121502583..121505992hg38UCSC Ensembl
chr9:124264862..124268271hg19UCSC Ensembl
Cytoband9q33.2
Allele length
AssemblyAllele length
hg383410
hg193410
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18279765
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6561034
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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