A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv2789016



Internal ID21234354
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:68816532..68818219hg38UCSC Ensembl
chr10:70576289..70577976hg19UCSC Ensembl
Cytoband10q21.3
Allele length
AssemblyAllele length
hg381688
hg191688
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv13693124
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nsv2789016
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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