A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18018747



Internal ID20585787
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:45259058..45264804hg38UCSC Ensembl
chr14:45728261..45734007hg19UCSC Ensembl
Cytoband14q21.2
Allele length
AssemblyAllele length
hg385747
hg195747
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6477234
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18018747
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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