A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6015057



Internal ID21924400
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:651839..651990hg38UCSC Ensembl
chr7:691476..691627hg19UCSC Ensembl
Cytoband7p22.3
Allele length
AssemblyAllele length
hg38152
hg19152
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17574622
Samples
Known GenesPRKAR1B
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6015057
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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