A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6035187



Internal ID21944530
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:70427498..70429310hg38UCSC Ensembl
chr14:70894215..70896027hg19UCSC Ensembl
Cytoband14q24.2
Allele length
AssemblyAllele length
hg381813
hg191813
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17598794
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6035187
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