A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5456441



Internal ID234508
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:43625014..43625829hg38UCSC Ensembl
chr6:43592751..43593566hg19UCSC Ensembl
Cytoband6p21.1
Allele length
AssemblyAllele length
hg38816
hg19816
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16981695
Samples
Known GenesGTPBP2
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5456441
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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