A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5616159



Internal ID21564464
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:131357263..131357263hg38UCSC Ensembl
chr3:131076107..131076107hg19UCSC Ensembl
Cytoband3q22.1
Allele length
AssemblyAllele length
hg3850
hg1950
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17137370, nssv17134866
SamplesNA18939, HG00513
Known GenesLOC339874
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5616159
Frequency
Sample Size35
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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