A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18234319



Internal ID20801360
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:57033537..57034509hg38UCSC Ensembl
chr12:57427321..57428293hg19UCSC Ensembl
Cytoband12q13.3
Allele length
AssemblyAllele length
hg38973
hg19973
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6584508
Supporting Variants
Samples
Known GenesMYO1A
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18234319
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer