A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5845649



Internal ID22620584
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:53990767..53994631hg38UCSC Ensembl
chr6:53855565..53859429hg19UCSC Ensembl
Cytoband6p12.1
Allele length
AssemblyAllele length
hg383865
hg193865
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17506512
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5845649
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