A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6595358



Internal ID20968429
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:16421216..16422324hg38UCSC Ensembl
chr17:16324530..16325638hg19UCSC Ensembl
Cytoband17p11.2
Allele length
AssemblyAllele length
hg381109
hg191109
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18242057
Samples
Known GenesTRPV2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6595358
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