A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6064753



Internal ID21973986
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:99410396..99410396hg38UCSC Ensembl
chr7:99008019..99008019hg19UCSC Ensembl
Cytoband7q22.1
Allele length
AssemblyAllele length
hg38313
hg19313
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17570993
Samples
Known GenesBUD31
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6064753
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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