A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5625591



Internal ID21573896
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:107072715..107072715hg38UCSC Ensembl
chr7:106713160..106713160hg19UCSC Ensembl
Cytoband7q22.3
Allele length
AssemblyAllele length
hg38324
hg19324
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17142826
SamplesNA19239
Known GenesPRKAR2B
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5625591
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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