A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6016551



Internal ID21925894
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:130450341..130457879hg38UCSC Ensembl
chr9:133325728..133333266hg19UCSC Ensembl
Cytoband9q34.11
Allele length
AssemblyAllele length
hg387539
hg197539
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17585512
Samples
Known GenesASS1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6016551
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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