A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18269592



Internal ID20836632
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:29659789..29660664hg38UCSC Ensembl
chr5:29659896..29660771hg19UCSC Ensembl
Cytoband5p13.3
Allele length
AssemblyAllele length
hg38876
hg19876
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6563474
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18269592
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