A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6580416



Internal ID20953487
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:79924190..79924241hg38UCSC Ensembl
chr12:80317970..80318021hg19UCSC Ensembl
Cytoband12q21.31
Allele length
AssemblyAllele length
hg3852
hg1952
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18232345
Samples
Known GenesPPP1R12A
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6580416
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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