A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3112445



Internal ID21295711
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:610559..633020hg38UCSC Ensembl
Innerchr7:650196..672657hg19UCSC Ensembl
Cytoband7p22.3
Allele length
AssemblyAllele length
hg3822462
hg1922462
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14084668
Samplessample224
Known GenesPRKAR1B
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3112445
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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