A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6485532



Internal ID21143085
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:37583501..37625800hg38UCSC Ensembl
chr14:38052706..38095005hg19UCSC Ensembl
Cytoband14q21.1
Allele length
AssemblyAllele length
hg3842300
hg1942300
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2101n223
Supporting Variantsnssv18177946
Samples
Known GenesFOXA1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6485532
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