A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6576702



Internal ID20949773
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:98476932..98479534hg38UCSC Ensembl
chr12:98870710..98873312hg19UCSC Ensembl
Cytoband12q23.1
Allele length
AssemblyAllele length
hg382603
hg192603
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18226308
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6576702
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