A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6449343



Internal ID21106896
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:3919188..3927319hg38UCSC Ensembl
chr11:3940418..3948549hg19UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg388132
hg198132
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17990781
Samples
Known GenesSTIM1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6449343
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