A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4760681



Internal ID20536542
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:142222658..142222658hg38UCSC Ensembl
chr6:142543795..142543795hg19UCSC Ensembl
Cytoband6q24.1
Allele length
AssemblyAllele length
hg38129
hg19129
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16292430
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4760681
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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