A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4767700



Internal ID20543560
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:168448354..168448354hg38UCSC Ensembl
chr6:168849034..168849034hg19UCSC Ensembl
Cytoband6q27
Allele length
AssemblyAllele length
hg3886
hg1986
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16293956
Samples
Known GenesSMOC2
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4767700
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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