A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6577793



Internal ID20950864
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:50362267..50362613hg38UCSC Ensembl
chr12:50756050..50756396hg19UCSC Ensembl
Cytoband12q13.12
Allele length
AssemblyAllele length
hg38347
hg19347
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18236922
Samples
Known GenesFAM186A
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6577793
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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