A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5867087



Internal ID22642022
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:38264247..38266496hg38UCSC Ensembl
chr14:38733452..38735701hg19UCSC Ensembl
Cytoband14q21.1
Allele length
AssemblyAllele length
hg382250
hg192250
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17468194
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5867087
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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