A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5872746



Internal ID22647687
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:39553370..39574022hg38UCSC Ensembl
chr18:37133334..37153986hg19UCSC Ensembl
Cytoband18q12.2
Allele length
AssemblyAllele length
hg3820653
hg1920653
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17479637
Samples
Known GenesLINC00669
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5872746
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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