A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18019720



Internal ID20586760
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:50029289..50035671hg38UCSC Ensembl
chr14:50496007..50502389hg19UCSC Ensembl
Cytoband14q21.3
Allele length
AssemblyAllele length
hg386383
hg196383
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6482730
Supporting Variants
Samples
Known GenesLOC100506499
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18019720
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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