A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17404612



Internal ID22462482
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:55159745..55159818hg38UCSC Ensembl
chr19:55671113..55671186hg19UCSC Ensembl
Cytoband19q13.42
Allele length
AssemblyAllele length
hg3874
hg1974
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5930160
Supporting Variants
Samples
Known GenesDNAAF3
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17404612
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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