A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5866809



Internal ID22641744
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:88442859..88457664hg38UCSC Ensembl
chr14:88909203..88924008hg19UCSC Ensembl
Cytoband14q31.3
Allele length
AssemblyAllele length
hg3814806
hg1914806
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17470339, nssv17469724
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5866809
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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