A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5459183



Internal ID237200
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:112886077..112886436hg38UCSC Ensembl
chr4:113807233..113807592hg19UCSC Ensembl
Cytoband4q25
Allele length
AssemblyAllele length
hg38360
hg19360
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16956023
Samples
Known GenesANK2
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5459183
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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