A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv13693124



Internal ID21214975
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 StatusS
Merged Variantsnsv2789016
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nssv13693124
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.03125


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