A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5989087



Internal ID21898430
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:27348568..27348645hg38UCSC Ensembl
chr2:27571435..27571512hg19UCSC Ensembl
Cytoband2p23.3
Allele length
AssemblyAllele length
hg3878
hg1978
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17533553
Samples
Known GenesGTF3C2
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv5989087
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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