A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6587594



Internal ID20960665
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:64019708..64020982hg38UCSC Ensembl
chr17:62097068..62098342hg19UCSC Ensembl
Cytoband17q23.3
Allele length
AssemblyAllele length
hg381275
hg191275
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18242632
Samples
Known GenesICAM2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6587594
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