A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17460113



Internal ID22517999
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:58121973..58128973hg38UCSC Ensembl
chr14:58588691..58595691hg19UCSC Ensembl
Cytoband14q23.1
Allele length
AssemblyAllele length
hg387001
hg197001
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5857599
Supporting Variants
Samples
Known GenesC14orf37
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17460113
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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