A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6482587



Internal ID21140140
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:69360676..69361276hg38UCSC Ensembl
chr14:69827393..69827993hg19UCSC Ensembl
Cytoband14q24.1
Allele length
AssemblyAllele length
hg38601
hg19601
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18020592
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6482587
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