A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5856794



Internal ID22631729
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:53536267..53543130hg38UCSC Ensembl
chr8:54448827..54455690hg19UCSC Ensembl
Cytoband8q11.23
Allele length
AssemblyAllele length
hg386864
hg196864
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17507411
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5856794
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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