A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6353255



Internal ID21010808
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:111159047..111161927hg38UCSC Ensembl
chr2:111916624..111919504hg19UCSC Ensembl
Cytoband2q13
Allele length
AssemblyAllele length
hg382881
hg192881
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18075401
Samples
Known GenesBCL2L11
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6353255
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