A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6000744



Internal ID21910087
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:97896728..97896911hg38UCSC Ensembl
chr9:100659010..100659193hg19UCSC Ensembl
Cytoband9q22.33
Allele length
AssemblyAllele length
hg38184
hg19184
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17593313
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6000744
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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