A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5618908



Internal ID21567213
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:237566132..237566132hg38UCSC Ensembl
chr2:238474775..238474775hg19UCSC Ensembl
Cytoband2q37.3
Allele length
AssemblyAllele length
hg38111
hg19111
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17111953
SamplesNA19239
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5618908
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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