A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6581464



Internal ID20954535
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:116701965..116702668hg38UCSC Ensembl
chr12:117139770..117140473hg19UCSC Ensembl
Cytoband12q24.22
Allele length
AssemblyAllele length
hg38704
hg19704
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18219140
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6581464
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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