A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6078027



Internal ID21987260
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:2546999..2546999hg38UCSC Ensembl
chr7:2586633..2586633hg19UCSC Ensembl
Cytoband7p22.3
Allele length
AssemblyAllele length
hg3852
hg1952
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17561596
Samples
Known GenesBRAT1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6078027
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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