A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17395619



Internal ID22453489
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:46052417..46058105hg38UCSC Ensembl
chr19:46555675..46561363hg19UCSC Ensembl
Cytoband19q13.32
Allele length
AssemblyAllele length
hg385689
hg195689
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5943885
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17395619
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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