A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4751969



Internal ID20527829
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:96516061..96516061hg38UCSC Ensembl
chr5:95851765..95851765hg19UCSC Ensembl
Cytoband5q15
Allele length
AssemblyAllele length
hg38870
hg19870
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16270644
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4751969
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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