A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6045106



Internal ID21954376
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:45710951..45710951hg38UCSC Ensembl
chr1:46176623..46176623hg19UCSC Ensembl
Cytoband1p34.1
Allele length
AssemblyAllele length
hg381185
hg191185
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17534472
Samples
Known GenesIPP
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6045106
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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