A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6004719



Internal ID21914062
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:11009746..11201012hg38UCSC Ensembl
chr9:11009746..11201012hg19UCSC Ensembl
Cytoband9p23
Allele length
AssemblyAllele length
hg38191267
hg19191267
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17583140
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6004719
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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