A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16286109



Internal ID20495327
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:30664207..30664267hg38UCSC Ensembl
chr19:31155114..31155174hg19UCSC Ensembl
Cytoband19q12
Allele length
AssemblyAllele length
hg3861
hg1961
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4731361
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16286109
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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