A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5846125



Internal ID22621060
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:88138672..88142221hg38UCSC Ensembl
chr6:88848391..88851940hg19UCSC Ensembl
Cytoband6q15
Allele length
AssemblyAllele length
hg383550
hg193550
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17508477
Samples
Known GenesCNR1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5846125
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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