A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5609700



Internal ID21558005
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:177432890..177432890hg38UCSC Ensembl
chr3:177150678..177150678hg19UCSC Ensembl
Cytoband3q26.32
Allele length
AssemblyAllele length
hg3861
hg1961
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17124103
SamplesHG00513
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5609700
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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