A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6047842



Internal ID21957075
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:167825568..167825568hg38UCSC Ensembl
chr1:167794806..167794806hg19UCSC Ensembl
Cytoband1q24.2
Allele length
AssemblyAllele length
hg38150
hg19150
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17520347
Samples
Known GenesADCY10
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6047842
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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