A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6050153



Internal ID21959387
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:16875179..16875243hg38UCSC Ensembl
chr19:16985990..16986054hg19UCSC Ensembl
Cytoband19p13.11
Allele length
AssemblyAllele length
hg3865
hg1965
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17622430
Samples
Known GenesSIN3B
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6050153
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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