A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5881384



Internal ID22656359
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:80227603..80231148hg38UCSC Ensembl
chr18:77985486..77989031hg19UCSC Ensembl
Cytoband18q23
Allele length
AssemblyAllele length
hg383546
hg193546
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17472587
Samples
Known GenesPARD6G
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5881384
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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