A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6468254



Internal ID21125807
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:119180901..119184600hg38UCSC Ensembl
chr11:119051610..119055309hg19UCSC Ensembl
Cytoband11q23.3
Allele length
AssemblyAllele length
hg383700
hg193700
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17986657
Samples
Known GenesNLRX1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6468254
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