A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17403225



Internal ID22461095
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:48929835..48936990hg38UCSC Ensembl
chr19:49433092..49440247hg19UCSC Ensembl
Cytoband19q13.33
Allele length
AssemblyAllele length
hg387156
hg197156
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5935755
Supporting Variants
Samples
Known GenesDHDH
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17403225
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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