A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6142000



Internal ID341200
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:65262000..65324200hg38UCSC Ensembl
chr9:70155606..70217806hg19UCSC Ensembl
Cytoband9q21.11
Allele length
AssemblyAllele length
hg3862201
hg1962201
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17024942
Samples
Known GenesFOXD4L5
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv6142000
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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