A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6569150



Internal ID20942221
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:37810156..37810501hg38UCSC Ensembl
chr9:37810153..37810498hg19UCSC Ensembl
Cytoband9p13.2
Allele length
AssemblyAllele length
hg38346
hg19346
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18280688
Samples
Known GenesDCAF10
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6569150
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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