A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4756116



Internal ID20531976
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:37982517..37982517hg38UCSC Ensembl
chr15:38274718..38274718hg19UCSC Ensembl
Cytoband15q14
Allele length
AssemblyAllele length
hg38141
hg19141
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16281183
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4756116
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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