A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6076167



Internal ID21985400
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:46977327..46977327hg38UCSC Ensembl
chr4:46979344..46979344hg19UCSC Ensembl
Cytoband4p12
Allele length
AssemblyAllele length
hg3875
hg1975
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17549208
Samples
Known GenesGABRA4
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6076167
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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