A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6439183



Internal ID21096736
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:17349029..17355868hg38UCSC Ensembl
chr11:17370576..17377415hg19UCSC Ensembl
Cytoband11p15.1
Allele length
AssemblyAllele length
hg386840
hg196840
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17988764
Samples
Known GenesNCR3LG1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6439183
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