A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6006134



Internal ID21915477
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:69773021..69773120hg38UCSC Ensembl
chr9:72387937..72388036hg19UCSC Ensembl
Cytoband9q21.12
Allele length
AssemblyAllele length
hg38100
hg19100
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17591008
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6006134
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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