A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17128694



Internal ID21465786
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:6369583..6369583hg38UCSC Ensembl
chr4:6371310..6371310hg19UCSC Ensembl
Cytoband4p16.1
Allele length
AssemblyAllele length
hg38500
hg19500
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5613140
Supporting Variants
SamplesHG03065
Known GenesPPP2R2C
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17128694
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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