A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16276441



Internal ID20485659
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:30952160..30952241hg38UCSC Ensembl
chr19:31443066..31443147hg19UCSC Ensembl
Cytoband19q12
Allele length
AssemblyAllele length
hg3882
hg1982
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4743449
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16276441
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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