A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6074426



Internal ID21983659
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:124281502..124281502hg38UCSC Ensembl
chr7:123921556..123921556hg19UCSC Ensembl
Cytoband7q31.33
Allele length
AssemblyAllele length
hg38179
hg19179
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17567975
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6074426
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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