A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5848660



Internal ID22623595
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:61930913..61939229hg38UCSC Ensembl
chr14:62397631..62405947hg19UCSC Ensembl
Cytoband14q23.2
Allele length
AssemblyAllele length
hg388317
hg198317
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17455305
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5848660
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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