A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5608926



Internal ID21557231
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:15272527..15272527hg38UCSC Ensembl
chr3:15314034..15314034hg19UCSC Ensembl
Cytoband3p25.1
Allele length
AssemblyAllele length
hg3864
hg1964
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17125569, nssv17135639
SamplesHG00731, NA18534
Known GenesSH3BP5
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5608926
Frequency
Sample Size35
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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