A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6592623



Internal ID20965694
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:22460715..22463234hg38UCSC Ensembl
chr12:22613649..22616168hg19UCSC Ensembl
Cytoband12p12.1
Allele length
AssemblyAllele length
hg382520
hg192520
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18231813
Samples
Known GenesC2CD5
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6592623
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