A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5542251



Internal ID316688
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:29904073..29904073hg38UCSC Ensembl
chr4:29905695..29905695hg19UCSC Ensembl
Cytoband4p15.1
Allele length
AssemblyAllele length
hg38170
hg19170
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16946465
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5542251
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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