A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5859188



Internal ID22634123
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:29437967..29445341hg38UCSC Ensembl
chr8:29295484..29302858hg19UCSC Ensembl
Cytoband8p12
Allele length
AssemblyAllele length
hg387375
hg197375
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17505926
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5859188
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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