A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17147131



Internal ID21464806
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:135956411..135956411hg38UCSC Ensembl
chr6:136277549..136277549hg19UCSC Ensembl
Cytoband6q23.3
Allele length
AssemblyAllele length
hg38737
hg19737
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5625419
Supporting Variants
SamplesHG03065
Known GenesPDE7B
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17147131
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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