A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6592611



Internal ID20965682
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:50371894..50372582hg38UCSC Ensembl
chr12:50765677..50766365hg19UCSC Ensembl
Cytoband12q13.12
Allele length
AssemblyAllele length
hg38689
hg19689
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18223534
Samples
Known GenesFAM186A
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6592611
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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