A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6556707



Internal ID20929778
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:116535662..116536662hg38UCSC Ensembl
chr3:116254509..116255509hg19UCSC Ensembl
Cytoband3q13.31
Allele length
AssemblyAllele length
hg381001
hg191001
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18261706
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6556707
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