A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4760467



Internal ID20536327
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:34361098..34361098hg38UCSC Ensembl
chr18:31941062..31941062hg19UCSC Ensembl
Cytoband18q12.1
Allele length
AssemblyAllele length
hg386040
hg196040
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16295031
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4760467
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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