A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17061245



Internal ID21432438
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:161035893..161035893hg38UCSC Ensembl
chr1:161005683..161005683hg19UCSC Ensembl
Cytoband1q23.3
Allele length
AssemblyAllele length
hg38432
hg19432
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5610251
Supporting Variants
SamplesHG00731
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17061245
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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