A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4754661



Internal ID20530521
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:21260124..21260124hg38UCSC Ensembl
chr14:21728283..21728283hg19UCSC Ensembl
Cytoband14q11.2
Allele length
AssemblyAllele length
hg38749
hg19749
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16290915
Samples
Known GenesHNRNPC
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4754661
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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