A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17065784



Internal ID21511800
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:43911562..43911562hg38UCSC Ensembl
chr1:44377234..44377234hg19UCSC Ensembl
Cytoband1p34.1
Allele length
AssemblyAllele length
hg38168
hg19168
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5623872
Supporting Variants
SamplesNA24385
Known GenesST3GAL3
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17065784
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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