A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6004447



Internal ID21913790
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:111951616..111956653hg38UCSC Ensembl
chr9:114713896..114718933hg19UCSC Ensembl
Cytoband9q31.3
Allele length
AssemblyAllele length
hg385038
hg195038
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17587596
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6004447
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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