A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5609679



Internal ID21557984
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:47140298..47140298hg38UCSC Ensembl
chr1:47605970..47605970hg19UCSC Ensembl
Cytoband1p33
Allele length
AssemblyAllele length
hg38248
hg19248
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17065969
SamplesHG02587
Known GenesCYP4A22
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5609679
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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