A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6006062



Internal ID21915405
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:40037296..40160445hg38UCSC Ensembl
chr7:40076895..40200044hg19UCSC Ensembl
Cytoband7p14.1
Allele length
AssemblyAllele length
hg38123150
hg19123150
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17566018
Samples
Known GenesC7orf10, CDK13, MPLKIP
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6006062
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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