A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6067643



Internal ID21976876
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:603614..603614hg38UCSC Ensembl
chr7:643251..643251hg19UCSC Ensembl
Cytoband7p22.3
Allele length
AssemblyAllele length
hg38168
hg19168
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17574222
Samples
Known GenesPRKAR1B
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6067643
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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