A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17159108



Internal ID21478793
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:125917196..125917196hg38UCSC Ensembl
chr6:126238342..126238342hg19UCSC Ensembl
Cytoband6q22.32
Allele length
AssemblyAllele length
hg383399
hg193399
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5638184
Supporting Variants
SamplesHG03486
Known GenesNCOA7
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17159108
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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