A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5882591



Internal ID22657568
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:80106891..80112419hg38UCSC Ensembl
chr18:77864775..77870302hg19UCSC Ensembl
Cytoband18q23
Allele length
AssemblyAllele length
hg385529
hg195528
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17479911
Samples
Known GenesADNP2
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5882591
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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