A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6018975



Internal ID21928318
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:74244620..74245282hg38UCSC Ensembl
chr7:73658950..73659612hg19UCSC Ensembl
Cytoband7q11.23
Allele length
AssemblyAllele length
hg38663
hg19663
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17565582
Samples
Known GenesRFC2
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6018975
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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