A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5610930



Internal ID21559235
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 StatusM
Merged Variants
Supporting Variantsnssv17066167
SamplesHG03732
Known GenesLINC00466
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5610930
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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