A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5439055



Internal ID217602
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:30190258..30200109hg38UCSC Ensembl
chr4:30191880..30201731hg19UCSC Ensembl
Cytoband4p15.1
Allele length
AssemblyAllele length
hg389852
hg199852
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16946490
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5439055
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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