A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4767666



Internal ID20543526
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:195337911..195337911hg38UCSC Ensembl
chr3:195058640..195058640hg19UCSC Ensembl
Cytoband3q29
Allele length
AssemblyAllele length
hg3888
hg1988
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16285776
Samples
Known GenesACAP2
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4767666
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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