A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17406799



Internal ID22464669
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:38297959..38301075hg38UCSC Ensembl
chr19:38788599..38791715hg19UCSC Ensembl
Cytoband19q13.2
Allele length
AssemblyAllele length
hg383117
hg193117
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5937416
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17406799
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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