A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5547237



Internal ID321108
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:19663867..19663917hg38UCSC Ensembl
chr11:19685413..19685463hg19UCSC Ensembl
Cytoband11p15.1
Allele length
AssemblyAllele length
hg38500
hg19500
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17044742
Samples
Known GenesNAV2
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5547237
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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