A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5649801



Internal ID21598106
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:29063391..29063391hg38UCSC Ensembl
chr15:29355594..29355594hg19UCSC Ensembl
Cytoband15q13.1
Allele length
AssemblyAllele length
hg38446
hg19446
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17094321
SamplesHG03125
Known GenesAPBA2
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5649801
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