A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5851694



Internal ID22626629
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:94798219..94801609hg38UCSC Ensembl
chr14:95264556..95267946hg19UCSC Ensembl
Cytoband14q32.13
Allele length
AssemblyAllele length
hg383391
hg193391
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17470180
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5851694
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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