A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5643893



Internal ID21592198
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:132674123..132674123hg38UCSC Ensembl
chr8:133686369..133686369hg19UCSC Ensembl
Cytoband8q24.22
Allele length
AssemblyAllele length
hg3869
hg1969
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17153254
SamplesHG03125
Known GenesLRRC6
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5643893
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