A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6591526



Internal ID20964597
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:103975812..103976242hg38UCSC Ensembl
chr12:104369590..104370020hg19UCSC Ensembl
Cytoband12q23.3
Allele length
AssemblyAllele length
hg38431
hg19431
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18226453
Samples
Known GenesTDG
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6591526
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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