A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5653351



Internal ID21601656
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:3649513..3649513hg38UCSC Ensembl
chr19:3649511..3649511hg19UCSC Ensembl
Cytoband19p13.3
Allele length
AssemblyAllele length
hg38150
hg19150
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17104951, nssv17104952
SamplesHG02011, HG00513
Known GenesPIP5K1C
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5653351
Frequency
Sample Size35
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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