A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6003806



Internal ID21913149
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:95766498..95766570hg38UCSC Ensembl
chr9:98528780..98528852hg19UCSC Ensembl
Cytoband9q22.32
Allele length
AssemblyAllele length
hg3873
hg1973
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17594318
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6003806
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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