A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6586074



Internal ID20959145
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:110558644..110559726hg38UCSC Ensembl
chr12:110996449..110997531hg19UCSC Ensembl
Cytoband12q24.11
Allele length
AssemblyAllele length
hg381083
hg191083
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18226335
Samples
Known GenesPPTC7
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6586074
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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