A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6580726



Internal ID20953797
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:8607902..8608407hg38UCSC Ensembl
chr12:8760498..8761003hg19UCSC Ensembl
Cytoband12p13.31
Allele length
AssemblyAllele length
hg38506
hg19506
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18223249
Samples
Known GenesAICDA
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6580726
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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