A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5862912



Internal ID22637847
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:38875761..38895183hg38UCSC Ensembl
chr14:39344965..39364387hg19UCSC Ensembl
Cytoband14q21.1
Allele length
AssemblyAllele length
hg3819423
hg1919423
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17458931
Samples
Known GenesLINC00639
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5862912
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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