A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17394801



Internal ID22452671
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:55558834..55570631hg38UCSC Ensembl
chr19:56070200..56081997hg19UCSC Ensembl
Cytoband19q13.42
Allele length
AssemblyAllele length
hg3811798
hg1911798
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5942229
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17394801
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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