A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16277923



Internal ID20487141
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:50592249..50592249hg38UCSC Ensembl
chr1:51057921..51057921hg19UCSC Ensembl
Cytoband1p32.3
Allele length
AssemblyAllele length
hg38307
hg19307
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4759744
Supporting Variants
Samples
Known GenesFAF1
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16277923
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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