A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17376104



Internal ID22601773
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:58492613..58502010hg38UCSC Ensembl
chr14:58959331..58968728hg19UCSC Ensembl
Cytoband14q23.1
Allele length
AssemblyAllele length
hg389398
hg199398
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5931776
Supporting Variants
Samples
Known GenesKIAA0586
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17376104
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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