A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6011845



Internal ID21921188
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:7484646..7877555hg38UCSC Ensembl
chr7:7524277..7917186hg19UCSC Ensembl
Cytoband7p21.3
Allele length
AssemblyAllele length
hg38392910
hg19392910
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17573287
Samples
Known GenesCOL28A1, MIOS, RPA3, RPA3-AS1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6011845
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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