A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5465432



Internal ID243294
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:39279820..39280486hg38UCSC Ensembl
chr4:39281440..39282106hg19UCSC Ensembl
Cytoband4p14
Allele length
AssemblyAllele length
hg38667
hg19667
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16947241
Samples
Known GenesMIR1273H, WDR19
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5465432
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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