A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5604559



Internal ID21553229
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:43338071..43338071hg38UCSC Ensembl
chr1:43803742..43803742hg19UCSC Ensembl
Cytoband1p34.2
Allele length
AssemblyAllele length
hg38365
hg19365
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17065369
SamplesNA18534
Known GenesMPL
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5604559
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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