A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17149196



Internal ID21422966
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:143630227..143630227hg38UCSC Ensembl
chr6:143951364..143951364hg19UCSC Ensembl
Cytoband6q24.2
Allele length
AssemblyAllele length
hg38317
hg19317
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5634408
Supporting Variants
SamplesHG00731
Known GenesPHACTR2
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17149196
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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