A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6485761



Internal ID21143314
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:21125665..21153768hg38UCSC Ensembl
chr14:21593824..21621927hg19UCSC Ensembl
Cytoband14q11.2
Allele length
AssemblyAllele length
hg3828104
hg1928104
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18016635
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6485761
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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