A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17398714



Internal ID22456584
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:39288671..39297593hg38UCSC Ensembl
chr19:39779311..39788233hg19UCSC Ensembl
Cytoband19q13.2
Allele length
AssemblyAllele length
hg388923
hg198923
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5944160
Supporting Variants
Samples
Known GenesIFNL1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17398714
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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