A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5871811



Internal ID22646749
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:31891533..31895527hg38UCSC Ensembl
chr20:30479336..30483330hg19UCSC Ensembl
Cytoband20q11.21
Allele length
AssemblyAllele length
hg383995
hg193995
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17485290
Samples
Known GenesTTLL9
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5871811
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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