A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17124154



Internal ID21458826
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:66570225..66570225hg38UCSC Ensembl
chr3:66620649..66620649hg19UCSC Ensembl
Cytoband3p14.1
Allele length
AssemblyAllele length
hg38319
hg19319
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5610356
Supporting Variants
SamplesHG02587
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17124154
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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