A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16284393



Internal ID20493611
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:241015631..241015631hg38UCSC Ensembl
chr2:241955048..241955048hg19UCSC Ensembl
Cytoband2q37.3
Allele length
AssemblyAllele length
hg38153
hg19153
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4757775
Supporting Variants
Samples
Known GenesSNED1
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16284393
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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