A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5656675



Internal ID21604980
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:41410414..41410414hg38UCSC Ensembl
chr13:41984550..41984550hg19UCSC Ensembl
Cytoband13q14.11
Allele length
AssemblyAllele length
hg383502
hg193502
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17090007
SamplesHG02587
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5656675
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