A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17060154



Internal ID21432031
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:119010728..119010728hg38UCSC Ensembl
chr1:119553351..119553351hg19UCSC Ensembl
Cytoband1p12
Allele length
AssemblyAllele length
hg381078
hg191078
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5605726
Supporting Variants
SamplesHG00731
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17060154
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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