A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18021817



Internal ID20588857
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:92281120..92281650hg38UCSC Ensembl
chr14:92747464..92747994hg19UCSC Ensembl
Cytoband14q32.12
Allele length
AssemblyAllele length
hg38531
hg19531
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6512054
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18021817
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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