A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6483842



Internal ID21141395
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:72626690..72627180hg38UCSC Ensembl
chr14:73093398..73093888hg19UCSC Ensembl
Cytoband14q24.2
Allele length
AssemblyAllele length
hg38491
hg19491
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18021058
Samples
Known GenesDPF3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6483842
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