A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5626071



Internal ID21574376
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:170368995..170368995hg38UCSC Ensembl
chr6:170678083..170678083hg19UCSC Ensembl
Cytoband6q27
Allele length
AssemblyAllele length
hg38132
hg19132
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17144116
SamplesHG00864
Known GenesFAM120B
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5626071
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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