A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16274389



Internal ID20483607
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:29719340..29719697hg38UCSC Ensembl
chr19:30210247..30210604hg19UCSC Ensembl
Cytoband19q12
Allele length
AssemblyAllele length
hg38358
hg19358
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4736688
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16274389
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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