A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5607562



Internal ID21555867
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:169167961..169167961hg38UCSC Ensembl
chr3:168885749..168885749hg19UCSC Ensembl
Cytoband3q26.2
Allele length
AssemblyAllele length
hg38311
hg19311
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17128076
SamplesHG00513
Known GenesMECOM
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5607562
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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