A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17059831



Internal ID21439071
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:1049124..1049124hg38UCSC Ensembl
chr1:984504..984504hg19UCSC Ensembl
Cytoband1p36.33
Allele length
AssemblyAllele length
hg38245
hg19245
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5610422
Supporting Variants
SamplesHG00732
Known GenesAGRN
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17059831
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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