A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5866770



Internal ID22641705
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:95978746..95983571hg38UCSC Ensembl
chr14:96445083..96449908hg19UCSC Ensembl
Cytoband14q32.2
Allele length
AssemblyAllele length
hg384826
hg194826
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv614n209
Supporting Variantsnssv17470202
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5866770
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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