A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18267506



Internal ID20834546
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:140650634..140651419hg38UCSC Ensembl
chr5:140030219..140031004hg19UCSC Ensembl
Cytoband5q31.3
Allele length
AssemblyAllele length
hg38786
hg19786
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6575068
Supporting Variants
Samples
Known GenesIK
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18267506
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