A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5856566



Internal ID22631501
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:27838486..27853967hg38UCSC Ensembl
chr9:27838484..27853965hg19UCSC Ensembl
Cytoband9p21.2
Allele length
AssemblyAllele length
hg3815482
hg1915482
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17512598
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5856566
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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