A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6587961



Internal ID20961032
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:75697464..75787201hg38UCSC Ensembl
chr16:75731362..75821099hg19UCSC Ensembl
Cytoband16q23.1
Allele length
AssemblyAllele length
hg3889738
hg1989738
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18240091
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6587961
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