A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5880401



Internal ID22655371
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:34119799..34121448hg38UCSC Ensembl
chr18:31699763..31701412hg19UCSC Ensembl
Cytoband18q12.1
Allele length
AssemblyAllele length
hg381650
hg191650
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17479618
Samples
Known GenesNOL4
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5880401
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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