A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5467224



Internal ID245042
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:57912141..57920124hg38UCSC Ensembl
chr4:58778307..58786290hg19UCSC Ensembl
Cytoband4q12
Allele length
AssemblyAllele length
hg387984
hg197984
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16951196
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5467224
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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