A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17061231



Internal ID21488368
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:160934960..160934960hg38UCSC Ensembl
chr1:160904750..160904750hg19UCSC Ensembl
Cytoband1q23.3
Allele length
AssemblyAllele length
hg3850
hg1950
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5622644
Supporting Variants
SamplesNA18939
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17061231
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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