A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5519005



Internal ID295364
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:44969856..44971000hg38UCSC Ensembl
chr19:45473113..45474257hg19UCSC Ensembl
Cytoband19q13.32
Allele length
AssemblyAllele length
hg381145
hg191145
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17725276
Samples
Known GenesCLPTM1
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5519005
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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