A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6541609



Internal ID20914891
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:42293703..42294631hg38UCSC Ensembl
chr2:42520843..42521771hg19UCSC Ensembl
Cytoband2p21
Allele length
AssemblyAllele length
hg38929
hg19929
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18257930
Samples
Known GenesEML4
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6541609
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