A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5457221



Internal ID235271
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:15656525..15658390hg38UCSC Ensembl
chr6:15656756..15658621hg19UCSC Ensembl
Cytoband6p22.3
Allele length
AssemblyAllele length
hg381866
hg191866
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16980657
Samples
Known GenesDTNBP1
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5457221
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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