A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5876212



Internal ID22651172
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:77084766..77087860hg38UCSC Ensembl
chr18:74796722..74799816hg19UCSC Ensembl
Cytoband18q23
Allele length
AssemblyAllele length
hg383095
hg193095
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17479838
Samples
Known GenesMBP
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5876212
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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