A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5644499



Internal ID21592804
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:122507958..122507958hg38UCSC Ensembl
chr10:124267474..124267474hg19UCSC Ensembl
Cytoband10q26.13
Allele length
AssemblyAllele length
hg38100
hg19100
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17068589
SamplesNA19238
Known GenesHTRA1
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5644499
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