A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4743566



Internal ID20519554
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:7953276..7953387hg38UCSC Ensembl
chr19:8018161..8018272hg19UCSC Ensembl
Cytoband19p13.2
Allele length
AssemblyAllele length
hg38112
hg19112
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16269824
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4743566
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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