A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16260428



Internal ID20469646
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:46635517..46635632hg38UCSC Ensembl
chr19:47138774..47138889hg19UCSC Ensembl
Cytoband19q13.32
Allele length
AssemblyAllele length
hg38116
hg19116
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4731210
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16260428
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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