A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6580609



Internal ID20953680
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:28987664..29000738hg38UCSC Ensembl
chr12:29140597..29153671hg19UCSC Ensembl
Cytoband12p11.22
Allele length
AssemblyAllele length
hg3813075
hg1913075
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18230751
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6580609
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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