A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6581629



Internal ID20954700
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:83832176..84528985hg38UCSC Ensembl
chr16:83865781..84562591hg19UCSC Ensembl
Cytoband16q23.3
Allele length
AssemblyAllele length
hg38696810
hg19696811
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18240854
Samples
Known GenesADAD2, ATP2C2, DNAAF1, HSDL1, KCNG4, MBTPS1, MLYCD, NECAB2, OSGIN1, SLC38A8, TAF1C, TLDC1, WFDC1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6581629
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