A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5948770



Internal ID22724233
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:6281166..6281166hg38UCSC Ensembl
chr10:6323129..6323129hg19UCSC Ensembl
Cytoband10p15.1
Allele length
AssemblyAllele length
hg38272
hg19272
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17363136
Samples
Known GenesLOC399715
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5948770
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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