A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17479459



Internal ID22537361
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:7357918..7367479hg38UCSC Ensembl
chr19:7422804..7432365hg19UCSC Ensembl
Cytoband19p13.2
Allele length
AssemblyAllele length
hg389562
hg199562
Variant TypeOTHER copy number variation
Copy Number2
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5876366
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17479459
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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