A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18018625



Internal ID20585665
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:41231463..41267335hg38UCSC Ensembl
chr14:41700666..41736538hg19UCSC Ensembl
Cytoband14q21.1
Allele length
AssemblyAllele length
hg3835873
hg1935873
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6489104
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18018625
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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