A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6580031



Internal ID20953102
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:118046308..118046782hg38UCSC Ensembl
chr12:118484113..118484587hg19UCSC Ensembl
Cytoband12q24.23
Allele length
AssemblyAllele length
hg38475
hg19475
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18223682
Samples
Known GenesWSB2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6580031
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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