A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5861793



Internal ID22636728
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:23090949..23098682hg38UCSC Ensembl
chr14:23560158..23567891hg19UCSC Ensembl
Cytoband14q11.2
Allele length
AssemblyAllele length
hg387734
hg197734
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17463855
Samples
Known GenesACIN1, C14orf119
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5861793
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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