A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5623746



Internal ID21572051
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:156804731..156804731hg38UCSC Ensembl
chr2:157661243..157661243hg19UCSC Ensembl
Cytoband2q24.1
Allele length
AssemblyAllele length
hg38327
hg19327
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17110355
SamplesNA19239
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5623746
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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