A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5466823



Internal ID244652
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:39484846..39486506hg38UCSC Ensembl
chr4:39486466..39488126hg19UCSC Ensembl
Cytoband4p14
Allele length
AssemblyAllele length
hg381661
hg191661
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16947257
Samples
Known GenesMIR1273H
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5466823
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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