A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5850077



Internal ID22625012
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:23229212..23230353hg38UCSC Ensembl
chr14:23698421..23699562hg19UCSC Ensembl
Cytoband14q11.2
Allele length
AssemblyAllele length
hg381142
hg191142
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17468763
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5850077
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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