A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6579372



Internal ID20952443
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:12185146..12185935hg38UCSC Ensembl
chr12:12338080..12338869hg19UCSC Ensembl
Cytoband12p13.2
Allele length
AssemblyAllele length
hg38790
hg19790
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18226902
Samples
Known GenesLRP6
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6579372
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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