A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5852802



Internal ID22627737
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:31288077..31311372hg38UCSC Ensembl
chr8:31145593..31168888hg19UCSC Ensembl
Cytoband8p12
Allele length
AssemblyAllele length
hg3823296
hg1923296
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17509131
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5852802
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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