A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16296206



Internal ID20505424
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:241487599..241487599hg38UCSC Ensembl
chr2:242427014..242427014hg19UCSC Ensembl
Cytoband2q37.3
Allele length
AssemblyAllele length
hg3853
hg1953
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4750917
Supporting Variants
Samples
Known GenesFARP2
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16296206
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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