A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4734018



Internal ID20509951
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:16875171..16875236hg38UCSC Ensembl
chr19:16985982..16986047hg19UCSC Ensembl
Cytoband19p13.11
Allele length
AssemblyAllele length
hg3866
hg1966
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16272571
Samples
Known GenesSIN3B
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4734018
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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