A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6006677



Internal ID21916020
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:651759..651914hg38UCSC Ensembl
chr7:691396..691551hg19UCSC Ensembl
Cytoband7p22.3
Allele length
AssemblyAllele length
hg38156
hg19156
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17558761
Samples
Known GenesPRKAR1B
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6006677
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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