A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5886919



Internal ID22661908
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:44713836..44719035hg38UCSC Ensembl
chr17:42791204..42796403hg19UCSC Ensembl
Cytoband17q21.31
Allele length
AssemblyAllele length
hg385200
hg195200
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17474385
Samples
Known GenesDBF4B
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5886919
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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