A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17389819



Internal ID22447689
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:6671447..6671748hg38UCSC Ensembl
chr19:6671458..6671759hg19UCSC Ensembl
Cytoband19p13.3
Allele length
AssemblyAllele length
hg38302
hg19302
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5939376
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17389819
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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