A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6591997



Internal ID20965068
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:38629735..41866813hg38UCSC Ensembl
chr12:39023537..42260615hg19UCSC Ensembl
Cytoband12q12
Allele length
AssemblyAllele length
hg383237079
hg193237079
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18237094
Samples
Known GenesABCD2, C12orf40, CNTN1, CPNE8, KIF21A, LRRK2, MUC19, PDZRN4, SLC2A13
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6591997
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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