A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6558616



Internal ID20931687
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:133093619..133094097hg38UCSC Ensembl
chr5:132429311..132429789hg19UCSC Ensembl
Cytoband5q31.1
Allele length
AssemblyAllele length
hg38479
hg19479
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5938n223
Supporting Variantsnssv18266687
Samples
Known GenesHSPA4
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6558616
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