A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6071498



Internal ID21980731
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:111166347..111166347hg38UCSC Ensembl
chr6:111487550..111487550hg19UCSC Ensembl
Cytoband6q21
Allele length
AssemblyAllele length
hg384479
hg194479
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17572506
Samples
Known GenesSLC16A10
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6071498
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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