A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5854178



Internal ID22629113
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:94765785..94769326hg38UCSC Ensembl
chr14:95232122..95235663hg19UCSC Ensembl
Cytoband14q32.13
Allele length
AssemblyAllele length
hg383542
hg193542
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17470177
Samples
Known GenesGSC
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5854178
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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