A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17062827



Internal ID21463669
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:222645833..222645833hg38UCSC Ensembl
chr1:222819175..222819175hg19UCSC Ensembl
Cytoband1q41
Allele length
AssemblyAllele length
hg38335
hg19335
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5622970
Supporting Variants
SamplesHG03009
Known GenesMIA3
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17062827
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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