A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18184880



Internal ID20751920
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:49946608..50011891hg38UCSC Ensembl
chr14:50413326..50478609hg19UCSC Ensembl
Cytoband14q21.3
Allele length
AssemblyAllele length
hg3865284
hg1965284
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6491321
Supporting Variants
Samples
Known GenesC14orf182, LOC100506499, MIR6076
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18184880
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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