A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5602714



Internal ID21551373
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:46635556..46635740hg38UCSC Ensembl
chr19:47138813..47138997hg19UCSC Ensembl
Cytoband19q13.32
Allele length
AssemblyAllele length
hg38185
hg19185
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17105343
SamplesHG03486
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5602714
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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