A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18242594



Internal ID20809634
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:62642695..62643030hg38UCSC Ensembl
chr17:60720056..60720391hg19UCSC Ensembl
Cytoband17q23.2
Allele length
AssemblyAllele length
hg38336
hg19336
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6587231
Supporting Variants
Samples
Known GenesMRC2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18242594
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer