A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5647893



Internal ID21596198
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:57319177..57319177hg38UCSC Ensembl
chr19:57830545..57830545hg19UCSC Ensembl
Cytoband19q13.43
Allele length
AssemblyAllele length
hg38130
hg19130
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17106475
SamplesHG00731
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5647893
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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