A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5918679



Internal ID22693901
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:25185156..25201895hg38UCSC Ensembl
chr10:25474085..25490824hg19UCSC Ensembl
Cytoband10p12.1
Allele length
AssemblyAllele length
hg3816740
hg1916740
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17364679
Samples
Known GenesGPR158
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5918679
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