A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5455123



Internal ID233207
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:175568610..175621774hg38UCSC Ensembl
chr4:176489761..176542925hg19UCSC Ensembl
Cytoband4q34.2
Allele length
AssemblyAllele length
hg3853165
hg1953165
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv385n206
Supporting Variantsnssv16959445
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5455123
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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