A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5637732



Internal ID21586037
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:23704136..23704136hg38UCSC Ensembl
chr9:23704134..23704134hg19UCSC Ensembl
Cytoband9p21.3
Allele length
AssemblyAllele length
hg38123
hg19123
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17161239
SamplesHG00731
Known GenesELAVL2
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5637732
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