A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6013819



Internal ID21923162
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:35645712..35645951hg38UCSC Ensembl
chr9:35645709..35645948hg19UCSC Ensembl
Cytoband9p13.3
Allele length
AssemblyAllele length
hg38240
hg19240
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17596742
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6013819
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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