A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5609925



Internal ID21558230
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:137919395..137919395hg38UCSC Ensembl
chr2:138676965..138676965hg19UCSC Ensembl
Cytoband2q22.1
Allele length
AssemblyAllele length
hg381407
hg191407
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17109257
SamplesHG03732
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5609925
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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