A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6070336



Internal ID21979569
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:125011861..125011861hg38UCSC Ensembl
chr8:126024103..126024103hg19UCSC Ensembl
Cytoband8q24.13
Allele length
AssemblyAllele length
hg38319
hg19319
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17583897
Samples
Known GenesSQLE
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6070336
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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