A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6562382



Internal ID20935453
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:129000347..129000781hg38UCSC Ensembl
chr9:131762626..131763060hg19UCSC Ensembl
Cytoband9q34.11
Allele length
AssemblyAllele length
hg38435
hg19435
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18280006
Samples
Known GenesNUP188
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6562382
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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