A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6594818



Internal ID20967889
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:31429829..31430381hg38UCSC Ensembl
chr17:29756847..29757399hg19UCSC Ensembl
Cytoband17q11.2
Allele length
AssemblyAllele length
hg38553
hg19553
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18242453
Samples
Known GenesRAB11FIP4
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6594818
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