A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6021022



Internal ID21930365
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:40356156..40356218hg38UCSC Ensembl
chr15:40648357..40648419hg19UCSC Ensembl
Cytoband15q15.1
Allele length
AssemblyAllele length
hg3863
hg1963
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17602503
Samples
Known GenesPHGR1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6021022
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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