A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5613871



Internal ID21562176
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:62272483..62272483hg38UCSC Ensembl
chr2:62499618..62499618hg19UCSC Ensembl
Cytoband2p15
Allele length
AssemblyAllele length
hg381029
hg191029
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17113359
SamplesHG03683
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5613871
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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