A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6015040



Internal ID21924383
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:955549..986801hg38UCSC Ensembl
chr7:995185..1026437hg19UCSC Ensembl
Cytoband7p22.3
Allele length
AssemblyAllele length
hg3831253
hg1931253
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17570559
Samples
Known GenesCOX19, CYP2W1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6015040
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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