A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4767825



Internal ID20543685
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:52497378..52497378hg38UCSC Ensembl
chr18:50023748..50023748hg19UCSC Ensembl
Cytoband18q21.2
Allele length
AssemblyAllele length
hg3860
hg1960
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16268089
Samples
Known GenesDCC
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4767825
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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