A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5617159



Internal ID21565464
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:65166588..65166588hg38UCSC Ensembl
chr2:65393722..65393722hg19UCSC Ensembl
Cytoband2p14
Allele length
AssemblyAllele length
hg38321
hg19321
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17114635
SamplesHG00732
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5617159
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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