A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6576619



Internal ID20949690
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:120406938..120408171hg38UCSC Ensembl
chr12:120844741..120845974hg19UCSC Ensembl
Cytoband12q24.31
Allele length
AssemblyAllele length
hg381234
hg191234
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18228075
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6576619
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