A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18224246



Internal ID20791286
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:11578527..11579086hg38UCSC Ensembl
chr12:11731461..11732020hg19UCSC Ensembl
Cytoband12p13.2
Allele length
AssemblyAllele length
hg38560
hg19560
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6582506
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18224246
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