A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6078958



Internal ID21988191
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:105268024..105268024hg38UCSC Ensembl
chr4:106189181..106189181hg19UCSC Ensembl
Cytoband4q24
Allele length
AssemblyAllele length
hg38300
hg19300
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17556670
Samples
Known GenesTET2
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6078958
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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