A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6589476



Internal ID20962547
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:55117613..55119296hg38UCSC Ensembl
chr12:55511397..55513080hg19UCSC Ensembl
Cytoband12q13.2
Allele length
AssemblyAllele length
hg381684
hg191684
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18230518
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6589476
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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