A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18179979



Internal ID20747019
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:34347322..34435602hg38UCSC Ensembl
chr14:34816528..34904808hg19UCSC Ensembl
Cytoband14q13.1
Allele length
AssemblyAllele length
hg3888281
hg1988281
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6479011
Supporting Variants
Samples
Known GenesSPTSSA
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18179979
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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