A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5847415



Internal ID22622350
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:695402..697201hg38UCSC Ensembl
chr7:735039..736838hg19UCSC Ensembl
Cytoband7p22.3
Allele length
AssemblyAllele length
hg381800
hg191800
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17501923
Samples
Known GenesPRKAR1B
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5847415
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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