A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6003901



Internal ID21913244
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:120597943..120600917hg38UCSC Ensembl
chr8:121610183..121613157hg19UCSC Ensembl
Cytoband8q24.12
Allele length
AssemblyAllele length
hg382975
hg192975
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17583568
Samples
Known GenesSNTB1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6003901
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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