A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6584188



Internal ID20957259
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:116061947..116062507hg38UCSC Ensembl
chr12:116499752..116500312hg19UCSC Ensembl
Cytoband12q24.21
Allele length
AssemblyAllele length
hg38561
hg19561
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18222228
Samples
Known GenesMED13L
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6584188
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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