A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17062360



Internal ID21407473
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:198841819..198841819hg38UCSC Ensembl
chr1:198810948..198810948hg19UCSC Ensembl
Cytoband1q32.1
Allele length
AssemblyAllele length
hg3858
hg1958
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5608334
Supporting Variants
SamplesHG00512
Known GenesMIR181A1HG
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17062360
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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