A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5594678



Internal ID21543278
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:11547083..11547185hg38UCSC Ensembl
chr19:11657898..11658000hg19UCSC Ensembl
Cytoband19p13.2
Allele length
AssemblyAllele length
hg38103
hg19103
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17103810
SamplesHG03125
Known GenesCNN1
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5594678
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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