A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18019169



Internal ID20586209
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:52185636..52205252hg38UCSC Ensembl
chr14:52652354..52671970hg19UCSC Ensembl
Cytoband14q22.1
Allele length
AssemblyAllele length
hg3819617
hg1919617
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6477103
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18019169
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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