A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5857599



Internal ID22632534
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:58121973..58128973hg38UCSC Ensembl
chr14:58588691..58595691hg19UCSC Ensembl
Cytoband14q23.1
Allele length
AssemblyAllele length
hg387001
hg197001
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17460113
Samples
Known GenesC14orf37
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5857599
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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