A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18182177



Internal ID20749217
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:55015768..55036485hg38UCSC Ensembl
chr14:55482486..55503203hg19UCSC Ensembl
Cytoband14q22.2
Allele length
AssemblyAllele length
hg3820718
hg1920718
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6486803
Supporting Variants
Samples
Known GenesSOCS4, WDHD1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18182177
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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