A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17532547



Internal ID21856903
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:1443737..1443804hg38UCSC Ensembl
chr2:1447509..1447576hg19UCSC Ensembl
Cytoband2p25.3
Allele length
AssemblyAllele length
hg3868
hg1968
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5986179
Supporting Variants
Samples
Known GenesTPO
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17532547
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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