A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6573936



Internal ID20947007
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:6372642..8080498hg38UCSC Ensembl
chr9:6372642..8080498hg19UCSC Ensembl
Cytoband9p24.1
Allele length
AssemblyAllele length
hg381707857
hg191707857
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18280771
Samples
Known GenesGLDC, KDM4C, TMEM261, UHRF2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6573936
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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