A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5477789



Internal ID255358
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:144779691..144785804hg38UCSC Ensembl
chr8:146005076..146011189hg19UCSC Ensembl
Cytoband8q24.3
Allele length
AssemblyAllele length
hg386114
hg196114
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17018472
Samples
Known GenesZNF34
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5477789
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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