A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4747868



Internal ID20523890
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:18879709..18879773hg38UCSC Ensembl
chr19:18990518..18990582hg19UCSC Ensembl
Cytoband19p13.11
Allele length
AssemblyAllele length
hg3865
hg1965
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16259848
Samples
Known GenesCERS1, GDF1
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4747868
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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