A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5861770



Internal ID22636705
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:92585314..92587513hg38UCSC Ensembl
chr14:93051659..93053858hg19UCSC Ensembl
Cytoband14q32.12
Allele length
AssemblyAllele length
hg382200
hg192200
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17470354
Samples
Known GenesRIN3
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5861770
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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