A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5862580



Internal ID22637515
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:68316197..68320246hg38UCSC Ensembl
chr11:68083665..68087714hg19UCSC Ensembl
Cytoband11q13.2
Allele length
AssemblyAllele length
hg384050
hg194050
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17469136
Samples
Known GenesLRP5
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5862580
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