A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5620939



Internal ID21569244
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:16194855..16194855hg38UCSC Ensembl
chr4:16196478..16196478hg19UCSC Ensembl
Cytoband4p15.32
Allele length
AssemblyAllele length
hg38110
hg19110
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17128073
SamplesNA19238
Known GenesTAPT1
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5620939
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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