A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17159091



Internal ID21407691
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:168309421..168309421hg38UCSC Ensembl
chr6:168710101..168710101hg19UCSC Ensembl
Cytoband6q27
Allele length
AssemblyAllele length
hg3858
hg1958
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5641137
Supporting Variants
SamplesHG00512
Known GenesDACT2
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17159091
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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