A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5435097



Internal ID213751
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:28473195..28477448hg38UCSC Ensembl
chr4:28474817..28479070hg19UCSC Ensembl
Cytoband4p15.1
Allele length
AssemblyAllele length
hg384254
hg194254
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16948638
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5435097
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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