A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5910645



Internal ID22685856
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:166221911..166221977hg38UCSC Ensembl
chr6:166635399..166635465hg19UCSC Ensembl
Cytoband6q27
Allele length
AssemblyAllele length
hg3867
hg1967
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17417759
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5910645
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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