A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5847799



Internal ID22622734
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:97700027..97709358hg38UCSC Ensembl
chr14:98166364..98175695hg19UCSC Ensembl
Cytoband14q32.2
Allele length
AssemblyAllele length
hg389332
hg199332
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17470217
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5847799
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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