A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18179508



Internal ID20746548
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:34622479..34628374hg38UCSC Ensembl
chr14:35091685..35097580hg19UCSC Ensembl
Cytoband14q13.1
Allele length
AssemblyAllele length
hg385896
hg195896
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6490501
Supporting Variants
Samples
Known GenesSNX6
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18179508
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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