A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18016691



Internal ID20583731
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:27462970..27592323hg38UCSC Ensembl
chr14:27932176..28061529hg19UCSC Ensembl
Cytoband14q12
Allele length
AssemblyAllele length
hg38129354
hg19129354
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6476263
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18016691
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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