A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5943303



Internal ID22718750
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:35905860..35911124hg38UCSC Ensembl
chr19:36396762..36402026hg19UCSC Ensembl
Cytoband19q13.12
Allele length
AssemblyAllele length
hg385265
hg195265
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17401976
Samples
Known GenesTYROBP
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5943303
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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