A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5926292



Internal ID22701519
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:23024012..23024729hg38UCSC Ensembl
chr10:23312941..23313658hg19UCSC Ensembl
Cytoband10p12.2
Allele length
AssemblyAllele length
hg38718
hg19718
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17362850
Samples
Known GenesARMC3
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5926292
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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