A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5929181



Internal ID22704430
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:16874386..16874442hg38UCSC Ensembl
chr19:16985197..16985253hg19UCSC Ensembl
Cytoband19p13.11
Allele length
AssemblyAllele length
hg3857
hg1957
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17394038
Samples
Known GenesSIN3B
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5929181
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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