A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6076793



Internal ID21986026
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:102256229..102256229hg38UCSC Ensembl
chr7:101899509..101899509hg19UCSC Ensembl
Cytoband7q22.1
Allele length
AssemblyAllele length
hg38534
hg19534
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17568486
Samples
Known GenesCUX1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6076793
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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