A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5864144



Internal ID22639079
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:83604471..83609210hg38UCSC Ensembl
chr8:84516706..84521445hg19UCSC Ensembl
Cytoband8q21.13
Allele length
AssemblyAllele length
hg384740
hg194740
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17510054
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5864144
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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