A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18016916



Internal ID20583957
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:26655653..26969392hg38UCSC Ensembl
chr14:27124859..27438598hg19UCSC Ensembl
Cytoband14q12
Allele length
AssemblyAllele length
hg38313740
hg19313740
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6477763
Supporting Variants
Samples
Known GenesMIR4307
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18016916
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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