A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17475382



Internal ID22533278
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:39288705..39297567hg38UCSC Ensembl
chr19:39779345..39788207hg19UCSC Ensembl
Cytoband19q13.2
Allele length
AssemblyAllele length
hg388863
hg198863
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5871154
Supporting Variants
Samples
Known GenesIFNL1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17475382
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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