A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5475691



Internal ID253326
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:140882480..140888255hg38UCSC Ensembl
chr7:140582280..140588055hg19UCSC Ensembl
Cytoband7q34
Allele length
AssemblyAllele length
hg385776
hg195776
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17004666
Samples
Known GenesBRAF
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5475691
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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