A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18196281



Internal ID20763321
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:58096961..58136077hg38UCSC Ensembl
chr14:58563679..58602795hg19UCSC Ensembl
Cytoband14q23.1
Allele length
AssemblyAllele length
hg3839117
hg1939117
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6480160
Supporting Variants
Samples
Known GenesC14orf37
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18196281
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer