A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4762499



Internal ID20538359
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:44518087..44518087hg38UCSC Ensembl
chr19:45022149..45022149hg19UCSC Ensembl
Cytoband19q13.31
Allele length
AssemblyAllele length
hg3857
hg1957
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16271085
Samples
Known GenesCEACAM20
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4762499
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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