A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6009806



Internal ID21919149
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:107144124..107145779hg38UCSC Ensembl
chr7:106784569..106786224hg19UCSC Ensembl
Cytoband7q22.3
Allele length
AssemblyAllele length
hg381656
hg191656
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17565030
Samples
Known GenesPRKAR2B
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6009806
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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