A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18234562



Internal ID20801602
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:91157674..91158751hg38UCSC Ensembl
chr12:91551451..91552528hg19UCSC Ensembl
Cytoband12q21.33
Allele length
AssemblyAllele length
hg381078
hg191078
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6592043
Supporting Variants
Samples
Known GenesDCN
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18234562
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.0002


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