A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17585238



Internal ID21777281
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 StatusS
Merged Variantsnsv6015069
Supporting Variants
Samples
Known GenesPHYHD1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17585238
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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