A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5980647



Internal ID21889990
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:107402274..107402340hg38UCSC Ensembl
chr1:107944896..107944962hg19UCSC Ensembl
Cytoband1p13.3
Allele length
AssemblyAllele length
hg3867
hg1967
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17533567
Samples
Known GenesNTNG1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv5980647
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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