A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6588493



Internal ID20961564
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:124887647..124888284hg38UCSC Ensembl
chr12:125372193..125372830hg19UCSC Ensembl
Cytoband12q24.31
Allele length
AssemblyAllele length
hg38638
hg19638
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18222435
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6588493
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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