A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6580657



Internal ID20953728
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:125260519..125262148hg38UCSC Ensembl
chr12:125745065..125746694hg19UCSC Ensembl
Cytoband12q24.31
Allele length
AssemblyAllele length
hg381630
hg191630
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18222982
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6580657
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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