A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5850027



Internal ID22624962
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:23220468..23228154hg38UCSC Ensembl
chr14:23689677..23697363hg19UCSC Ensembl
Cytoband14q11.2
Allele length
AssemblyAllele length
hg387687
hg197687
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17459741
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5850027
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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