A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5607059



Internal ID21555364
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:149764542..149764542hg38UCSC Ensembl
chr3:149482329..149482329hg19UCSC Ensembl
Cytoband3q25.1
Allele length
AssemblyAllele length
hg3885
hg1985
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17126437
SamplesHG00731
Known GenesANKUB1
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5607059
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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