A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4748786



Internal ID20524813
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:3143876..3144053hg38UCSC Ensembl
chr19:3143874..3144051hg19UCSC Ensembl
Cytoband19p13.3
Allele length
AssemblyAllele length
hg38178
hg19178
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16266998
Samples
Known GenesGNA15
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4748786
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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