A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17392437



Internal ID22450307
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:39228142..39228883hg38UCSC Ensembl
chr19:39718782..39719523hg19UCSC Ensembl
Cytoband19q13.2
Allele length
AssemblyAllele length
hg38742
hg19742
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5942334
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17392437
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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