A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6571285



Internal ID20944356
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:113329782..113330244hg38UCSC Ensembl
chr9:116092062..116092524hg19UCSC Ensembl
Cytoband9q32
Allele length
AssemblyAllele length
hg38463
hg19463
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18279641
Samples
Known GenesWDR31
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6571285
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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