A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17403130



Internal ID22461000
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:52233123..52236096hg38UCSC Ensembl
chr19:52736376..52739349hg19UCSC Ensembl
Cytoband19q13.41
Allele length
AssemblyAllele length
hg382974
hg192974
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5929567
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17403130
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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