A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5933484



Internal ID22708797
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:4830000..4830179hg38UCSC Ensembl
chr19:4830012..4830191hg19UCSC Ensembl
Cytoband19p13.3
Allele length
AssemblyAllele length
hg38180
hg19180
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17392028
Samples
Known GenesTICAM1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5933484
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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