A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6046766



Internal ID21955999
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:168725215..168725215hg38UCSC Ensembl
chr1:168694453..168694453hg19UCSC Ensembl
Cytoband1q24.2
Allele length
AssemblyAllele length
hg3855
hg1955
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17518989
Samples
Known GenesDPT
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6046766
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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