A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5618389



Internal ID21566694
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:234622865..234622865hg38UCSC Ensembl
chr2:235531509..235531509hg19UCSC Ensembl
Cytoband2q37.1
Allele length
AssemblyAllele length
hg3857
hg1957
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17111977
SamplesNA19239
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5618389
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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