A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5887321



Internal ID22662313
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:20958623..20961431hg38UCSC Ensembl
chr18:18538584..18541392hg19UCSC Ensembl
Cytoband18q11.1
Allele length
AssemblyAllele length
hg382809
hg192809
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17477781
Samples
Known GenesROCK1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5887321
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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