A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv612n209



Internal ID22826687
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:90789883..90801917hg38UCSC Ensembl
chr14:91256227..91268261hg19UCSC Ensembl
Cytoband14q32.11
Allele length
AssemblyAllele length
hg3812035
hg1912035
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv5930533, nsv5937290
Samples
Known GenesTTC7B
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)dgv612n209
Frequency
Sample Size914
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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