A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4767107



Internal ID20542967
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:3016161..3016161hg38UCSC Ensembl
chr18:3016159..3016159hg19UCSC Ensembl
Cytoband18p11.31
Allele length
AssemblyAllele length
hg3853
hg1953
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16290459
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4767107
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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