A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4432868



Internal ID21394870
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:55145153..55147718hg38UCSC Ensembl
chr19:55656521..55659086hg19UCSC Ensembl
Cytoband19q13.42
Allele length
AssemblyAllele length
hg382566
hg192566
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15747444
SamplesBTQ055
Known GenesTNNT1
MethodSequencing
Analysis
Platform
Comments
ReferenceDeng_et_al_2019
Pubmed ID31718558
Accession Number(s)nsv4432868
Frequency
Sample Size15
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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