A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5848222



Internal ID22623157
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:144873827..144884989hg38UCSC Ensembl
chr8:146099212..146110374hg19UCSC Ensembl
Cytoband8q24.3
Allele length
AssemblyAllele length
hg3811163
hg1911163
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17507661
Samples
Known GenesZNF250
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5848222
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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