A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17623023



Internal ID21815070
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:3445723..3445787hg38UCSC Ensembl
chr18:3445721..3445785hg19UCSC Ensembl
Cytoband18p11.31
Allele length
AssemblyAllele length
hg3865
hg1965
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6024123
Supporting Variants
Samples
Known GenesTGIF1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17623023
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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