A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4751962



Internal ID20527822
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:56720012..56720012hg38UCSC Ensembl
chr3:56754040..56754040hg19UCSC Ensembl
Cytoband3p14.3
Allele length
AssemblyAllele length
hg3897
hg1997
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16277942
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4751962
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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