A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6480624



Internal ID21138177
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:64359154..64374142hg38UCSC Ensembl
chr14:64825872..64840860hg19UCSC Ensembl
Cytoband14q23.3
Allele length
AssemblyAllele length
hg3814989
hg1914989
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18182587
Samples
Known GenesMIR548AZ
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6480624
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