A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5461287



Internal ID239244
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:102662563..102663176hg38UCSC Ensembl
chr4:103583720..103584333hg19UCSC Ensembl
Cytoband4q24
Allele length
AssemblyAllele length
hg38614
hg19614
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16953450
Samples
Known GenesMANBA
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5461287
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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