A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6572754



Internal ID20945825
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:38179363..38179570hg38UCSC Ensembl
chr8:38036881..38037088hg19UCSC Ensembl
Cytoband8p11.23
Allele length
AssemblyAllele length
hg38208
hg19208
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18277905
Samples
Known GenesBAG4
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6572754
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