A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6363465



Internal ID21021018
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:121014201..121015100hg38UCSC Ensembl
chr3:120733048..120733947hg19UCSC Ensembl
Cytoband3q13.33
Allele length
AssemblyAllele length
hg38900
hg19900
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18093629
Samples
Known GenesSTXBP5L
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6363465
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