A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6571393



Internal ID20944464
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:40836127..40840215hg38UCSC Ensembl
chr6:40803866..40807954hg19UCSC Ensembl
Cytoband6p21.1
Allele length
AssemblyAllele length
hg384089
hg194089
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18271431
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6571393
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