A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6436098



Internal ID21093651
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:17037001..17073900hg38UCSC Ensembl
chr11:17058548..17095447hg19UCSC Ensembl
Cytoband11p15.1
Allele length
AssemblyAllele length
hg3836900
hg1936900
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17988744
Samples
Known GenesOR7E14P
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6436098
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