A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5616574



Internal ID21564879
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:188602164..188602164hg38UCSC Ensembl
chr3:188319952..188319952hg19UCSC Ensembl
Cytoband3q28
Allele length
AssemblyAllele length
hg38118
hg19118
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17138243
SamplesHG00731
Known GenesLPP
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5616574
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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