A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5866413



Internal ID22641348
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:21599318..21604489hg38UCSC Ensembl
chr14:22067458..22072640hg19UCSC Ensembl
Cytoband14q11.2
Allele length
AssemblyAllele length
hg385172
hg195183
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17467635
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5866413
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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