A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6592228



Internal ID20965299
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:67611613..67613005hg38UCSC Ensembl
chr17:65607729..65609121hg19UCSC Ensembl
Cytoband17q24.2
Allele length
AssemblyAllele length
hg381393
hg191393
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18243783
Samples
Known GenesPITPNC1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6592228
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