A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17406527



Internal ID22464397
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:2357230..2357518hg38UCSC Ensembl
chr19:2357228..2357516hg19UCSC Ensembl
Cytoband19p13.3
Allele length
AssemblyAllele length
hg38289
hg19289
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5942862
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17406527
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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