A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6015126



Internal ID21924469
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:603707..603785hg38UCSC Ensembl
chr7:643344..643422hg19UCSC Ensembl
Cytoband7p22.3
Allele length
AssemblyAllele length
hg3879
hg1979
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17562741
Samples
Known GenesPRKAR1B
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6015126
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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