A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6444249



Internal ID21101802
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:1866119..1928522hg38UCSC Ensembl
chr11:1887349..1949752hg19UCSC Ensembl
Cytoband11p15.5
Allele length
AssemblyAllele length
hg3862404
hg1962404
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18194063
Samples
Known GenesLSP1, TNNT3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6444249
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