A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6578319



Internal ID20951390
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:60805641..60806059hg38UCSC Ensembl
chr17:58883002..58883420hg19UCSC Ensembl
Cytoband17q23.2
Allele length
AssemblyAllele length
hg38419
hg19419
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18243117
Samples
Known GenesBCAS3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6578319
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