A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5856474



Internal ID22631409
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:43989857..43997542hg38UCSC Ensembl
chr15:44282055..44289740hg19UCSC Ensembl
Cytoband15q15.3
Allele length
AssemblyAllele length
hg387686
hg197686
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17471862
Samples
Known GenesFRMD5
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5856474
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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