A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17065369



Internal ID21487389
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 StatusS
Merged Variantsnsv5604559
Supporting Variants
SamplesNA18534
Known GenesMPL
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17065369
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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