A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5644729



Internal ID21593034
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:67291397..67291397hg38UCSC Ensembl
chr11:67058868..67058868hg19UCSC Ensembl
Cytoband11q13.2
Allele length
AssemblyAllele length
hg38655
hg19655
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17075744
SamplesHG01114
Known GenesANKRD13D
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5644729
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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