A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5863045



Internal ID22637980
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:47763663..47764925hg38UCSC Ensembl
chr8:48676224..48677486hg19UCSC Ensembl
Cytoband8q11.21
Allele length
AssemblyAllele length
hg381263
hg191263
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17506778, nssv17506777
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5863045
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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