A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16279552



Internal ID20488770
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:33356252..33356252hg38UCSC Ensembl
chr1:33821853..33821853hg19UCSC Ensembl
Cytoband1p35.1
Allele length
AssemblyAllele length
hg3857
hg1957
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4763370
Supporting Variants
Samples
Known GenesPHC2
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16279552
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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