A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5854918



Internal ID22629853
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:123381661..123383817hg38UCSC Ensembl
chr8:124393901..124396057hg19UCSC Ensembl
Cytoband8q24.13
Allele length
AssemblyAllele length
hg382157
hg192157
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17506179
Samples
Known GenesATAD2
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5854918
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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