A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18020145



Internal ID20587185
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:63156457..63173819hg38UCSC Ensembl
chr14:63623175..63640537hg19UCSC Ensembl
Cytoband14q23.2
Allele length
AssemblyAllele length
hg3817363
hg1917363
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6493839
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18020145
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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