A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5470436



Internal ID248195
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:94127706..94176872hg38UCSC Ensembl
chr4:95048857..95098023hg19UCSC Ensembl
Cytoband4q22.2
Allele length
AssemblyAllele length
hg3849167
hg1949167
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16952774
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5470436
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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