A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6589029



Internal ID20962100
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:117873020..117873528hg38UCSC Ensembl
chr12:118310825..118311333hg19UCSC Ensembl
Cytoband12q24.23
Allele length
AssemblyAllele length
hg38509
hg19509
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18221185
Samples
Known GenesKSR2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6589029
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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