A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6011822



Internal ID21921165
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:36861195..36861265hg38UCSC Ensembl
chr9:36861192..36861262hg19UCSC Ensembl
Cytoband9p13.2
Allele length
AssemblyAllele length
hg3871
hg1971
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17577581
Samples
Known GenesPAX5
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6011822
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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