A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6475895



Internal ID21133448
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:76645776..76746476hg38UCSC Ensembl
chr14:77112119..77212819hg19UCSC Ensembl
Cytoband14q24.3
Allele length
AssemblyAllele length
hg38100701
hg19100701
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18182132
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6475895
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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