A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4762003



Internal ID20537863
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:14116101..14116101hg38UCSC Ensembl
chr4:14117725..14117725hg19UCSC Ensembl
Cytoband4p15.33
Allele length
AssemblyAllele length
hg3863
hg1963
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16265782
Samples
Known GenesLINC01085
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4762003
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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