A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5623639



Internal ID21571944
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:139416423..139416423hg38UCSC Ensembl
chr3:139135265..139135265hg19UCSC Ensembl
Cytoband3q23
Allele length
AssemblyAllele length
hg386050
hg196050
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17120757
SamplesHG00096
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5623639
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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