A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4749903



Internal ID20525938
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:69843440..69843497hg38UCSC Ensembl
chr9:72458356..72458413hg19UCSC Ensembl
Cytoband9q21.12
Allele length
AssemblyAllele length
hg3858
hg1958
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16277632
Samples
Known GenesC9orf135
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4749903
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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