A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6492788



Internal ID21150341
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:23226191..23236408hg38UCSC Ensembl
chr14:23695400..23705617hg19UCSC Ensembl
Cytoband14q11.2
Allele length
AssemblyAllele length
hg3810218
hg1910218
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18016728
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6492788
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