A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6483677



Internal ID21141230
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:74422668..74423693hg38UCSC Ensembl
chr14:74889371..74890396hg19UCSC Ensembl
Cytoband14q24.3
Allele length
AssemblyAllele length
hg381026
hg191026
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18021471
Samples
Known GenesSYNDIG1L
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6483677
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