A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6586072



Internal ID20959143
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:29889329..29890898hg38UCSC Ensembl
chr17:28216347..28217916hg19UCSC Ensembl
Cytoband17q11.2
Allele length
AssemblyAllele length
hg381570
hg191570
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18241736
Samples
Known GenesSSH2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6586072
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