A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4764649



Internal ID20540509
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:40766254..40766254hg38UCSC Ensembl
chr19:41272159..41272159hg19UCSC Ensembl
Cytoband19q13.2
Allele length
AssemblyAllele length
hg3873
hg1973
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16289150
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4764649
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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