A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6015069



Internal ID21924412
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:128934783..128945228hg38UCSC Ensembl
chr9:131697062..131707507hg19UCSC Ensembl
Cytoband9q34.11
Allele length
AssemblyAllele length
hg3810446
hg1910446
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17585238
Samples
Known GenesPHYHD1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6015069
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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