A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4762047



Internal ID20537907
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:41049276..41049276hg38UCSC Ensembl
chr4:41051293..41051293hg19UCSC Ensembl
Cytoband4p14
Allele length
AssemblyAllele length
hg38114
hg19114
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16262447
Samples
Known GenesAPBB2
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4762047
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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