A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17059814



Internal ID21487053
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:11770151..11770151hg38UCSC Ensembl
chr1:11830208..11830208hg19UCSC Ensembl
Cytoband1p36.22
Allele length
AssemblyAllele length
hg381313
hg191313
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5614259
Supporting Variants
SamplesNA12878
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17059814
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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