A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17066167



Internal ID21482569
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:63177455..63177455hg38UCSC Ensembl
chr1:63643126..63643126hg19UCSC Ensembl
Cytoband1p31.3
Allele length
AssemblyAllele length
hg3863
hg1963
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5610930
Supporting Variants
SamplesHG03732
Known GenesLINC00466
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17066167
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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