A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6589584



Internal ID20962655
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:116146211..116146753hg38UCSC Ensembl
chr12:116584016..116584558hg19UCSC Ensembl
Cytoband12q24.21
Allele length
AssemblyAllele length
hg38543
hg19543
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18232098
Samples
Known GenesMED13L
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6589584
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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