A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5836684



Internal ID22611619
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:56573571..56583309hg38UCSC Ensembl
chr3:56607599..56617337hg19UCSC Ensembl
Cytoband3p14.3
Allele length
AssemblyAllele length
hg389739
hg199739
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17493307
Samples
Known GenesCCDC66
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5836684
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