A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6492307



Internal ID21149860
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:46859469..46860263hg38UCSC Ensembl
chr13:47433604..47434398hg19UCSC Ensembl
Cytoband13q14.2
Allele length
AssemblyAllele length
hg38795
hg19795
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18008551
Samples
Known GenesHTR2A
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6492307
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer