A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6079153



Internal ID21988386
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:118970008..118970008hg38UCSC Ensembl
chr6:119291173..119291173hg19UCSC Ensembl
Cytoband6q22.31
Allele length
AssemblyAllele length
hg3860
hg1960
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17570524
Samples
Known GenesFAM184A
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6079153
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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