A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6589435



Internal ID20962506
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:37656716..37656902hg38UCSC Ensembl
chr17:36016745..36016931hg19UCSC Ensembl
Cytoband17q12
Allele length
AssemblyAllele length
hg38187
hg19187
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18242864
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6589435
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