A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17062271



Internal ID21475152
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:21129497..21129497hg38UCSC Ensembl
chr1:21455990..21455990hg19UCSC Ensembl
Cytoband1p36.12
Allele length
AssemblyAllele length
hg38351
hg19351
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5609413
Supporting Variants
SamplesHG03371
Known GenesEIF4G3
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17062271
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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