A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6581364



Internal ID20954435
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:50543825..50544581hg38UCSC Ensembl
chr12:50937608..50938364hg19UCSC Ensembl
Cytoband12q13.12
Allele length
AssemblyAllele length
hg38757
hg19757
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18234708
Samples
Known GenesDIP2B
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6581364
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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