A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5857540



Internal ID22632475
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:69549058..69552698hg38UCSC Ensembl
chr12:69942838..69946478hg19UCSC Ensembl
Cytoband12q15
Allele length
AssemblyAllele length
hg383641
hg193641
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17457897
Samples
Known GenesFRS2
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5857540
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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