A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5664004



Internal ID21612309
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:5910815..5910815hg38UCSC Ensembl
chr19:5910826..5910826hg19UCSC Ensembl
Cytoband19p13.3
Allele length
AssemblyAllele length
hg38324
hg19324
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17106527
SamplesHG00732
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5664004
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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