A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5878920



Internal ID22653887
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:179733762..179754845hg38UCSC Ensembl
chr1:179702897..179723980hg19UCSC Ensembl
Cytoband1q25.2
Allele length
AssemblyAllele length
hg3821084
hg1921084
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17362388
Samples
Known GenesFAM163A
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5878920
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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