A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5615898



Internal ID21564203
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:164213994..164213994hg38UCSC Ensembl
chr2:165070504..165070504hg19UCSC Ensembl
Cytoband2q24.3
Allele length
AssemblyAllele length
hg38331
hg19331
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17109676
SamplesHG02818
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5615898
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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