A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6038668



Internal ID21948011
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:100166041..100166108hg38UCSC Ensembl
chr14:100632378..100632445hg19UCSC Ensembl
Cytoband14q32.2
Allele length
AssemblyAllele length
hg3868
hg1968
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17600229
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6038668
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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