A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5457308



Internal ID235356
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:42316192..42316275hg38UCSC Ensembl
chr6:42283930..42284013hg19UCSC Ensembl
Cytoband6p21.1
Allele length
AssemblyAllele length
hg3884
hg1984
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16981619
Samples
Known GenesTRERF1
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5457308
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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