A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18192176



Internal ID20759216
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:94699263..94703327hg38UCSC Ensembl
chr14:95165600..95169664hg19UCSC Ensembl
Cytoband14q32.13
Allele length
AssemblyAllele length
hg384065
hg194065
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6506376
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18192176
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