A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4762648



Internal ID20538508
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:6868733..6868733hg38UCSC Ensembl
chr5:6868846..6868846hg19UCSC Ensembl
Cytoband5p15.31
Allele length
AssemblyAllele length
hg381339
hg191339
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16259632
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4762648
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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