A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18270331



Internal ID20837371
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:9863518..9864351hg38UCSC Ensembl
chr5:9863630..9864463hg19UCSC Ensembl
Cytoband5p15.2
Allele length
AssemblyAllele length
hg38834
hg19834
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6562885
Supporting Variants
Samples
Known GenesLOC285692
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18270331
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