A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6447857



Internal ID21105410
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:10871884..10937031hg38UCSC Ensembl
chr11:10893431..10958578hg19UCSC Ensembl
Cytoband11p15.3
Allele length
AssemblyAllele length
hg3865148
hg1965148
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18194709
Samples
Known GenesZBED5-AS1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6447857
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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