A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5648107



Internal ID21596412
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:34213168..34213168hg38UCSC Ensembl
chr19:34704073..34704073hg19UCSC Ensembl
Cytoband19q13.11
Allele length
AssemblyAllele length
hg38315
hg19315
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17104463
SamplesNA19239
Known GenesLSM14A
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5648107
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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