A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6573574



Internal ID20946645
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:10280937..10282766hg38UCSC Ensembl
chr5:10281049..10282878hg19UCSC Ensembl
Cytoband5p15.2
Allele length
AssemblyAllele length
hg381830
hg191830
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5637n223
Supporting Variantsnssv18266464
Samples
Known GenesCMBL
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6573574
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