A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17565582



Internal ID21757547
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 StatusS
Merged Variantsnsv6018975
Supporting Variants
Samples
Known GenesRFC2
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17565582
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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