A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6074503



Internal ID21983736
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:140909964..140909964hg38UCSC Ensembl
chr7:140609764..140609764hg19UCSC Ensembl
Cytoband7q34
Allele length
AssemblyAllele length
hg38306
hg19306
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17565495
Samples
Known GenesBRAF
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6074503
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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