A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17475953



Internal ID22533851
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:41187500..41191782hg38UCSC Ensembl
chr19:41693405..41697687hg19UCSC Ensembl
Cytoband19q13.2
Allele length
AssemblyAllele length
hg384283
hg194283
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5874666
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17475953
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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