A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17637123



Internal ID21829170
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:4308730..4308859hg38UCSC Ensembl
chr19:4308727..4308856hg19UCSC Ensembl
Cytoband19p13.3
Allele length
AssemblyAllele length
hg38130
hg19130
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6051239
Supporting Variants
Samples
Known GenesFSD1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17637123
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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