A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5466214



Internal ID244059
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:41595316..41596627hg38UCSC Ensembl
chr6:41563054..41564365hg19UCSC Ensembl
Cytoband6p21.1
Allele length
AssemblyAllele length
hg381312
hg191312
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16983159
Samples
Known GenesFOXP4
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5466214
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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