A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5845645



Internal ID22620580
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:53318565..53321214hg38UCSC Ensembl
chr6:53183363..53186012hg19UCSC Ensembl
Cytoband6p12.1
Allele length
AssemblyAllele length
hg382650
hg192650
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17506498
Samples
Known GenesELOVL5
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5845645
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