A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv15704856



Internal ID21377132
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:46466303..46466394hg38UCSC Ensembl
chr10:47083056..47083147hg19UCSC Ensembl
Cytoband10q11.22
Allele length
AssemblyAllele length
hg3892
hg1992
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4389358
Supporting Variants
Samples
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceWong_et_al_2019
Pubmed ID31340865
Accession Number(s)nssv15704856
Frequency
Sample Size174
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.0804598


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