A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5613565



Internal ID21561870
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:238296315..238296315hg38UCSC Ensembl
chr2:239204956..239204956hg19UCSC Ensembl
Cytoband2q37.3
Allele length
AssemblyAllele length
hg382484
hg192484
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17112031
SamplesNA19238
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5613565
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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