A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18180802



Internal ID20747842
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:44852618..44894822hg38UCSC Ensembl
chr14:45321821..45364025hg19UCSC Ensembl
Cytoband14q21.2
Allele length
AssemblyAllele length
hg3842205
hg1942205
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6483626
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18180802
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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