A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6578726



Internal ID20951797
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:65740321..65742578hg38UCSC Ensembl
chr15:66032659..66034916hg19UCSC Ensembl
Cytoband15q22.31
Allele length
AssemblyAllele length
hg382258
hg192258
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18238909
Samples
Known GenesDENND4A
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6578726
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