A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5851860



Internal ID22626795
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:38863661..38870860hg38UCSC Ensembl
chr14:39332865..39340064hg19UCSC Ensembl
Cytoband14q21.1
Allele length
AssemblyAllele length
hg387200
hg197200
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17458842
Samples
Known GenesLINC00639
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5851860
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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