A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4763321



Internal ID20539181
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:14774683..14774683hg38UCSC Ensembl
chr19:14885495..14885495hg19UCSC Ensembl
Cytoband19p13.12
Allele length
AssemblyAllele length
hg38275
hg19275
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16289254
Samples
Known GenesEMR2
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4763321
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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