A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4753313



Internal ID20529173
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:170087915..170087915hg38UCSC Ensembl
chr4:171009066..171009066hg19UCSC Ensembl
Cytoband4q33
Allele length
AssemblyAllele length
hg3852
hg1952
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16259647
Samples
Known GenesAADAT
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4753313
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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