A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5457841



Internal ID235877
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:140681553..140936446hg38UCSC Ensembl
chr6:141002690..141257583hg19UCSC Ensembl
Cytoband6q24.1
Allele length
AssemblyAllele length
hg38254894
hg19254894
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16970259
Samples
Known GenesMIR4465
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5457841
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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